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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:Somatosensory Disorders
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Accession:DOID:9008625 term browser browse the term
Definition:Disorders of sensory information received from superficial and deep regions of the body. The somatosensory system conveys neural impulses which pertain to proprioception, tactile sensation, thermal sensation, pressure sensation, and pain. PERIPHERAL NERVOUS SYSTEM DISEASES; SPINAL CORD DISEASES; and BRAIN DISEASES may be associated with impaired or abnormal somatic sensation.
Synonyms:exact_synonym: Light Touch Sensation Impairment;   Pain Sensation Diminished;   Pain Sensation Diminisheds;   Pinprick Sensation Diminished;   Pinprick Sensation Diminisheds;   Position Sense Disorder;   Position Sense Disorders;   Proprioceptive Disorder;   Proprioceptive Disorders;   Somatic Sensation Disorder;   Somatic Sensation Disorders;   Somatosensory Disorder;   Thermal Sensation Disorder;   Thermal Sensation Disorders
 primary_id: MESH:D020886;   RDO:0005828
For additional species annotation, visit the Alliance of Genome Resources.


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Somatosensory Disorders term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G CSF3 colony stimulating factor 3 EXP CTD Direct Evidence: marker/mechanism CTD PMID:7543699 NCBI chr17:40,015,440...40,017,813
Ensembl chr17:40,015,361...40,017,813
JBrowse link
G TTPA alpha tocopherol transfer protein EXP CTD Direct Evidence: marker/mechanism CTD PMID:10896705 NCBI chr 8:63,059,488...63,086,523
Ensembl chr 8:63,048,553...63,086,053
JBrowse link
chromosome 13q14 deletion syndrome term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G ACOD1 aconitate decarboxylase 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:76,948,511...76,958,638
Ensembl chr13:76,948,511...76,958,638
JBrowse link
G AL139082.1 novel transcript, antisense to NEK3 & NEK5 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,128,895...52,132,723
Ensembl chr13:52,128,891...52,132,723
JBrowse link
G AL355390.1 novel transcript IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:74,412,957...74,419,115
Ensembl chr13:74,412,957...74,419,115
JBrowse link
G AL445209.1 novel transcript, antisense to POU4F1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:78,596,122...78,599,619
Ensembl chr13:78,596,129...78,599,619
JBrowse link
G AL445238.1 keratin-associated protein 21-1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:63,832,361...63,833,053
Ensembl chr13:63,832,361...63,833,531
JBrowse link
G AL450447.1 putative UPF0607 protein ENSP00000383144 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:77,661,374...77,662,803
Ensembl chr13:77,661,376...77,662,626
JBrowse link
G ALG11 ALG11 alpha-1,2-mannosyltransferase IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,012,398...52,033,600
Ensembl chr13:52,012,398...52,033,600
JBrowse link
G ARL11 ADP ribosylation factor like GTPase 11 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,628,456...49,633,872
Ensembl chr13:49,628,507...49,633,872
JBrowse link
G ATP7B ATPase copper transporting beta IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:51,932,669...52,012,130
Ensembl chr13:51,930,436...52,012,125
JBrowse link
G ATXN8OS ATXN8 opposite strand lncRNA IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:70,107,213...70,139,753
Ensembl chr13:70,107,213...70,149,092
JBrowse link
G BORA BORA aurora kinase A activator IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:72,727,923...72,756,196
Ensembl chr13:72,727,749...72,756,198
JBrowse link
G C13orf42 chromosome 13 open reading frame 42 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:51,082,119...51,172,388
Ensembl chr13:51,082,119...51,200,252
JBrowse link
G CAB39L calcium binding protein 39 like IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,308,650...49,444,851
Ensembl chr13:49,308,650...49,444,064
JBrowse link
G CCDC70 coiled-coil domain containing 70 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:51,861,969...51,866,232
Ensembl chr13:51,861,981...51,866,232
JBrowse link
G CDADC1 cytidine and dCMP deaminase domain containing 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,247,875...49,293,486
Ensembl chr13:49,247,925...49,293,485
JBrowse link
G CKAP2 cytoskeleton associated protein 2 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,455,429...52,476,627
Ensembl chr13:52,455,429...52,476,628
JBrowse link
G CLN5 CLN5 intracellular trafficking protein IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:76,992,081...77,005,117
Ensembl chr13:76,990,660...77,019,143
JBrowse link
G CNMD chondromodulin IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,703,264...52,739,820
Ensembl chr13:52,703,264...52,739,820
JBrowse link
G COMMD6 COMM domain containing 6 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:75,525,214...75,549,439
Ensembl chr13:75,525,219...75,549,439
JBrowse link
G CYSLTR2 cysteinyl leukotriene receptor 2 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:48,653,929...48,711,226
Ensembl chr13:48,653,711...48,711,226
JBrowse link
G DACH1 dachshund family transcription factor 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:71,437,966...71,868,068
Ensembl chr13:71,437,966...71,867,204
JBrowse link
G DHRS12 dehydrogenase/reductase 12 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:51,767,993...51,804,163
Ensembl chr13:51,767,993...51,804,162
JBrowse link
G DIAPH3 diaphanous related formin 3 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:59,665,583...60,163,928
Ensembl chr13:59,665,583...60,163,928
JBrowse link
G DIAPH3-AS1 DIAPH3 antisense RNA 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:60,012,718...60,044,357
Ensembl chr13:60,012,734...60,044,357
JBrowse link
G DIAPH3-AS2 DIAPH3 antisense RNA 2 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:60,144,698...60,153,505
Ensembl chr13:60,144,648...60,153,678
JBrowse link
G DIS3 DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:72,752,169...72,781,900
Ensembl chr13:72,752,169...72,782,096
JBrowse link
G DLEU1 deleted in lymphocytic leukemia 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:50,082,169...50,528,643
Ensembl chr13:50,082,169...50,906,856
JBrowse link
G DLEU1-AS1 DLEU1 antisense RNA 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:50,520,933...50,527,449
Ensembl chr13:50,519,364...50,843,939
JBrowse link
G DLEU2 deleted in lymphocytic leukemia 2 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,982,549...50,125,541
Ensembl chr13:49,956,670...50,125,720
JBrowse link
G DLEU7 deleted in lymphocytic leukemia 7 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:50,711,026...50,843,945
Ensembl chr13:50,519,364...50,843,939
JBrowse link
G DLEU7-AS1 DLEU7 antisense RNA 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:50,807,855...50,849,905
Ensembl chr13:50,082,169...50,906,856
JBrowse link
G EBPL EBP like IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,660,674...49,691,487
Ensembl chr13:49,660,674...49,691,486
JBrowse link
G EDNRB endothelin receptor type B IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:77,895,481...77,975,527
Ensembl chr13:77,895,481...77,975,529
JBrowse link
G EDNRB-AS1 EDNRB antisense RNA 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:77,818,937...77,908,442
Ensembl chr13:77,779,723...77,844,145
JBrowse link
G FAM124A family with sequence similarity 124 member A IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:51,222,367...51,284,241
Ensembl chr13:51,222,334...51,284,241
Ensembl chr13:51,222,334...51,284,241
JBrowse link
G FBXL3 F-box and leucine rich repeat protein 3 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:76,992,597...77,027,164
Ensembl chr13:76,992,598...77,027,195
JBrowse link
G FNDC3A fibronectin type III domain containing 3A IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:48,975,241...49,209,779
Ensembl chr13:48,975,912...49,209,779
JBrowse link
G HNRNPA1L2 heterogeneous nuclear ribonucleoprotein A1 like 2 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,617,525...52,643,773
Ensembl chr13:52,642,425...52,643,796
JBrowse link
G INTS6 integrator complex subunit 6 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:51,353,171...51,453,333
Ensembl chr13:51,354,077...51,454,264
JBrowse link
G INTS6-AS1 INTS6 antisense RNA 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:51,453,345...51,454,716
Ensembl chr13:51,452,364...51,554,678
JBrowse link
G ITM2B integral membrane protein 2B IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:48,233,206...48,270,357
Ensembl chr13:48,232,612...48,270,357
JBrowse link
G KCNRG potassium channel regulator IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:50,015,444...50,020,922
Ensembl chr13:50,015,254...50,020,922
JBrowse link
G KCTD12 potassium channel tetramerization domain containing 12 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:76,880,175...76,886,405
Ensembl chr13:76,880,175...76,886,405
JBrowse link
G KLF12 Kruppel like factor 12 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:73,686,089...74,168,295
Ensembl chr13:73,686,089...73,995,056
JBrowse link
G KLF5 Kruppel like factor 5 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:73,054,976...73,077,538
Ensembl chr13:73,054,976...73,077,541
JBrowse link
G KLHL1 kelch like family member 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:69,700,593...70,108,452
Ensembl chr13:69,700,594...70,108,493
JBrowse link
G KPNA3 karyopherin subunit alpha 3 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,699,307...49,792,682
Ensembl chr13:49,699,320...49,792,682
JBrowse link
G LINC00331 long intergenic non-protein coding RNA 331 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:78,787,319...78,840,050
Ensembl chr13:78,786,272...78,840,051
JBrowse link
G LINC00333 long intergenic non-protein coding RNA 333 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:84,140,602...84,606,768
Ensembl chr13:84,562,364...84,563,236
JBrowse link
G LINC00345 long intergenic non-protein coding RNA 345 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,483,687...52,601,006
Ensembl chr13:52,482,804...52,489,216
JBrowse link
G LINC00347 long intergenic non-protein coding RNA 347 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:74,552,843...74,557,120
Ensembl chr13:74,552,503...74,565,445
JBrowse link
G LINC00348 long intergenic non-protein coding RNA 348 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:71,015,141...71,168,417
Ensembl chr13:71,015,042...71,168,417
JBrowse link
G LINC00351 long intergenic non-protein coding RNA 351 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:85,363,603...85,544,662
Ensembl chr13:85,363,601...85,544,570
JBrowse link
G LINC00355 long intergenic non-protein coding RNA 355 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:63,986,371...64,076,011
Ensembl chr13:63,851,197...64,076,044
JBrowse link
G LINC00358 long intergenic non-protein coding RNA 358 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:62,003,525...62,029,548
Ensembl chr13:61,997,136...62,029,572
JBrowse link
G LINC00364 long intergenic non-protein coding RNA 364 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:67,372,387...67,379,994
Ensembl chr13:67,326,177...67,379,994
JBrowse link
G LINC00374 long intergenic non-protein coding RNA 374 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:58,211,697...58,233,117
Ensembl chr13:58,211,697...58,233,117
JBrowse link
G LINC00375 long intergenic non-protein coding RNA 375 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:85,065,087...85,148,057
Ensembl chr13:85,065,087...85,078,920
JBrowse link
G LINC00376 long intergenic non-protein coding RNA 376 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:63,183,101...63,328,094
Ensembl chr13:63,183,096...63,328,129
JBrowse link
G LINC00377 long intergenic non-protein coding RNA 377 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:81,018,391...81,044,442
Ensembl chr13:81,018,176...81,044,691
JBrowse link
G LINC00378 long intergenic non-protein coding RNA 378 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:60,672,955...60,695,806
Ensembl chr13:60,618,991...61,176,758
JBrowse link
G LINC00381 long intergenic non-protein coding RNA 381 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:74,419,173...74,435,159
Ensembl chr13:74,419,158...74,444,735
JBrowse link
G LINC00382 long intergenic non-protein coding RNA 382 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:79,872,586...79,918,036
Ensembl chr13:79,872,586...79,918,042
JBrowse link
G LINC00383 long intergenic non-protein coding RNA 383 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:69,222,346...69,322,101
Ensembl chr13:69,221,866...69,322,190
JBrowse link
G LINC00392 long intergenic non-protein coding RNA 392 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:73,564,244...73,587,879
Ensembl chr13:73,564,244...73,588,070
JBrowse link
G LINC00393 long intergenic non-protein coding RNA 393 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:73,546,687...73,670,457
Ensembl chr13:73,413,473...73,661,891
JBrowse link
G LINC00395 long intergenic non-protein coding RNA 395 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:63,667,682...63,738,018
Ensembl chr13:63,667,681...63,738,018
JBrowse link
G LINC00402 long intergenic non-protein coding RNA 402 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:74,231,444...74,259,976
Ensembl chr13:74,231,457...74,259,976
JBrowse link
G LINC00430 long intergenic non-protein coding RNA 430 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:86,909,601...86,936,807
Ensembl chr13:86,909,586...86,937,108
JBrowse link
G LINC00434 long intergenic non-protein coding RNA 434 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:60,214,347...60,268,104
Ensembl chr13:60,214,352...60,214,946
JBrowse link
G LINC00444 long intergenic non-protein coding RNA 444 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:47,903,806...47,935,824 JBrowse link
G LINC00446 long intergenic non-protein coding RNA 446 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:78,012,883...78,053,595
Ensembl chr13:77,997,909...78,053,604
JBrowse link
G LINC00448 long intergenic non-protein coding RNA 448 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:62,672,285...62,807,359
Ensembl chr13:62,672,285...62,796,714
JBrowse link
G LINC00458 long intergenic non-protein coding RNA 458 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:54,124,324...54,132,871
Ensembl chr13:54,115,783...54,142,319
JBrowse link
G LINC00459 long intergenic non-protein coding RNA 459 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:62,323,657...62,328,847
Ensembl chr13:62,323,657...62,328,833
JBrowse link
G LINC00462 long intergenic non-protein coding RNA 462 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:48,576,974...48,580,901
Ensembl chr13:48,576,974...48,578,088
JBrowse link
G LINC00550 long intergenic non-protein coding RNA 550 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:68,861,284...68,885,325
Ensembl chr13:68,861,284...68,885,325
JBrowse link
G LINC00558 long intergenic non-protein coding RNA 558 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:53,815,419...53,876,119
Ensembl chr13:53,815,419...53,939,960
JBrowse link
G LINC00561 long intergenic non-protein coding RNA 561 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:75,932,398...75,935,132
Ensembl chr13:75,932,395...75,935,132
JBrowse link
G LINC00562 long intergenic non-protein coding RNA 562 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:47,930,153...47,932,622
Ensembl chr13:47,930,153...47,932,622
JBrowse link
G LINC00564 long intergenic non-protein coding RNA 564 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:81,225,865...81,226,983
Ensembl chr13:81,225,865...81,226,983
JBrowse link
G LINC01038 long intergenic non-protein coding RNA 1038 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:79,804,386...79,805,682
Ensembl chr13:79,804,418...79,805,685
JBrowse link
G LINC01052 long intergenic non-protein coding RNA 1052 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:65,866,047...65,878,219
Ensembl chr13:65,866,070...65,922,731
JBrowse link
G LINC01065 long intergenic non-protein coding RNA 1065 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:53,131,746...53,151,900
Ensembl chr13:53,099,397...53,151,914
JBrowse link
G LINC01068 long intergenic non-protein coding RNA 1068 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:79,566,727...79,571,446
Ensembl chr13:79,566,678...79,571,445
JBrowse link
G LINC01069 long intergenic non-protein coding RNA 1069 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:77,979,766...77,994,773
Ensembl chr13:77,979,817...77,997,881
JBrowse link
G LINC01074 long intergenic non-protein coding RNA 1074 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:62,321,305...62,322,398
Ensembl chr13:62,321,305...62,322,398
JBrowse link
G LINC01075 long intergenic non-protein coding RNA 1075 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:62,212,282...62,249,951
Ensembl chr13:62,212,577...62,249,947
JBrowse link
G LINC01077 long intergenic non-protein coding RNA 1077 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:48,567,598...48,570,464
Ensembl chr13:48,570,639...48,573,317
JBrowse link
G LINC01078 long intergenic non-protein coding RNA 1078 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:75,240,588...75,252,012
Ensembl chr13:75,250,480...75,252,012
JBrowse link
G LINC01080 long intergenic non-protein coding RNA 1080 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:80,011,077...80,026,663
Ensembl chr13:80,011,077...80,028,283
JBrowse link
G LINC01442 long intergenic non-protein coding RNA 1442 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:60,789,787...60,941,768
Ensembl chr13:60,916,981...60,945,955
JBrowse link
G LINC02333 long intergenic non-protein coding RNA 2333 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,334,295...52,341,883
Ensembl chr13:52,334,295...52,341,896
JBrowse link
G LINC02338 long intergenic non-protein coding RNA 2338 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:58,165,827...58,209,483
Ensembl chr13:58,165,827...58,209,483
JBrowse link
G LINC02339 long intergenic non-protein coding RNA 2339 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:61,424,689...61,427,946
Ensembl chr13:61,424,689...61,427,946
JBrowse link
G LMO7 LIM domain 7 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:75,620,434...75,859,870
Ensembl chr13:75,620,434...75,859,870
JBrowse link
G LMO7-AS1 LMO7 antisense RNA 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:75,604,700...75,635,994
Ensembl chr13:75,604,700...75,635,994
JBrowse link
G LMO7DN LMO7 downstream neighbor IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:75,871,038...75,883,813
Ensembl chr13:75,871,038...75,883,811
JBrowse link
G LMO7DN-IT1 LMO7DN intronic transcript 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:75,876,886...75,881,127
Ensembl chr13:75,876,886...75,881,127
JBrowse link
G LOC105370203 uncharacterized LOC105370203 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,235,513...49,247,840 JBrowse link
G LOC105370268 lncRNA-ACOD1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar
G LOC107457599 meiotic recombination hotspot P IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:60,690,561...60,694,062 JBrowse link
G LOC107882127 EDNRB upstream promoter region IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:77,975,613...77,976,074 JBrowse link
G LOC107882129 EDNRB proximal promoter region IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:77,918,760...77,919,832 JBrowse link
G LOC109461478 ATXN8 opposite strand (non-protein coding) repeat instability region IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:70,139,352...70,139,429 JBrowse link
G LOC110120827 VISTA enhancer hs126 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:70,769,477...70,770,736 JBrowse link
G LOC110120828 VISTA enhancer hs129 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:71,200,716...71,201,236 JBrowse link
G LOC110120829 VISTA enhancer hs131 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:72,197,133...72,199,738 JBrowse link
G LOC110120830 VISTA enhancer hs135 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:72,574,916...72,575,890 JBrowse link
G LOC110120831 VISTA enhancer hs137 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:71,726,717...71,728,802 JBrowse link
G LOC110120832 VISTA enhancer hs138 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:71,851,655...71,854,203 JBrowse link
G LOC110120833 VISTA enhancer hs141 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:72,426,945...72,428,915 JBrowse link
G LOC110120834 VISTA enhancer hs142 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:72,507,309...72,509,616 JBrowse link
G LOC110120843 VISTA enhancer hs188 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:71,771,848...71,774,098 JBrowse link
G LOC110120891 VISTA enhancer hs540 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:70,783,961...70,785,375 JBrowse link
G LOC110120897 VISTA enhancer hs575 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:67,854,985...67,856,394 JBrowse link
G LOC110120909 VISTA enhancer hs619 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:71,759,384...71,760,856 JBrowse link
G LOC110120945 VISTA enhancer hs881 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:66,035,667...66,036,616 JBrowse link
G LOC110120946 VISTA enhancer hs882 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:70,958,905...70,960,063 JBrowse link
G LOC110120950 VISTA enhancer hs915 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:78,401,880...78,403,203 JBrowse link
G LOC110121360 VISTA enhancer hs1394 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:77,831,993...77,833,579 JBrowse link
G LOC110121375 VISTA enhancer hs1471 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:79,658,111...79,660,495 JBrowse link
G LOC111365190 HNF1 motif-containing MPRA enhancer 52 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:74,227,924...74,228,068 JBrowse link
G LOC112163662 Sharpr-MPRA regulatory region 3717 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:48,066,562...48,066,947 JBrowse link
G LOC112163663 Sharpr-MPRA regulatory region 2352 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,104,673...52,104,967 JBrowse link
G LOC112163664 Sharpr-MPRA regulatory region 8029 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,850,374...52,850,668 JBrowse link
G LOC112163665 Sharpr-MPRA regulatory region 4317 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:60,584,335...60,584,629 JBrowse link
G LOC112163666 Sharpr-MPRA regulatory region 1301 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:63,625,916...63,626,210 JBrowse link
G LOC112163667 Sharpr-MPRA regulatory region 14942 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:68,057,157...68,057,451 JBrowse link
G LOC112163668 Sharpr-MPRA regulatory region 2769 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:73,090,471...73,090,765 JBrowse link
G LOC112163669 Sharpr-MPRA regulatory region 11269 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:74,187,632...74,187,926 JBrowse link
G LOC112163670 Sharpr-MPRA regulatory region 2285 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:74,287,712...74,288,006 JBrowse link
G LOC112163671 Sharpr-MPRA regulatory region 1150 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:77,409,474...77,409,768 JBrowse link
G LOC112163672 Sharpr-MPRA regulatory region 2923 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:84,399,374...84,399,668 JBrowse link
G LOC113939939 Sharpr-MPRA regulatory region 13963 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,301,133...49,301,427 JBrowse link
G LPAR6 lysophosphatidic acid receptor 6 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:48,400,897...48,444,669
Ensembl chr13:48,389,567...48,444,704
JBrowse link
G MED4 mediator complex subunit 4 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:48,075,724...48,095,104
Ensembl chr13:48,053,323...48,095,131
JBrowse link
G MED4-AS1 MED4 antisense RNA 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:48,077,137...48,079,993
Ensembl chr13:48,077,137...48,079,991
JBrowse link
G MIR1297 microRNA 1297 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:54,311,972...54,312,048
Ensembl chr13:54,311,972...54,312,048
JBrowse link
G MIR15A microRNA 15a IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:50,049,119...50,049,201
Ensembl chr13:50,049,119...50,049,201
JBrowse link
G MIR16-1 microRNA 16-1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:50,048,973...50,049,061
Ensembl chr13:50,048,973...50,049,061
JBrowse link
G MIR3169 microRNA 3169 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:61,199,798...61,199,880
Ensembl chr13:61,199,798...61,199,880
JBrowse link
G MIR3613 microRNA 3613 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,996,415...49,996,501
Ensembl chr13:49,996,415...49,996,501
JBrowse link
G MIR3665 microRNA 3665 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:77,698,012...77,698,116
Ensembl chr13:77,698,012...77,698,116
JBrowse link
G MIR4703 microRNA 4703 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:51,552,589...51,552,667
Ensembl chr13:51,552,589...51,552,667
JBrowse link
G MIR4704 microRNA 4704 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:66,218,250...66,218,324
Ensembl chr13:66,218,250...66,218,324
JBrowse link
G MIR5007 microRNA 5007 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:55,174,454...55,174,548
Ensembl chr13:55,174,454...55,174,548
JBrowse link
G MIR548X2 microRNA 548x-2 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:65,966,330...65,966,429
Ensembl chr13:65,966,330...65,966,429
JBrowse link
G MIR5693 microRNA 5693 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:51,348,567...51,348,639
Ensembl chr13:51,348,567...51,348,639
JBrowse link
G MIR759 microRNA 759 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,810,050...52,810,140
Ensembl chr13:52,810,050...52,810,140
JBrowse link
G MLNR motilin receptor IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,220,338...49,222,377
Ensembl chr13:49,220,338...49,222,377
JBrowse link
G MYCBP2 MYC binding protein 2 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:77,044,657...77,327,098
Ensembl chr13:77,044,657...77,327,094
JBrowse link
G MYCBP2-AS1 MYCBP2 antisense RNA 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:77,075,514...77,087,776
Ensembl chr13:77,026,767...77,129,717
JBrowse link
G MZT1 mitotic spindle organizing protein 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:72,708,367...72,727,629
Ensembl chr13:72,708,367...72,727,629
JBrowse link
G NDFIP2 Nedd4 family interacting protein 2 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:79,480,722...79,556,077
Ensembl chr13:79,481,124...79,556,075
JBrowse link
G NDFIP2-AS1 NDFIP2 antisense RNA 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:79,477,364...79,481,231
Ensembl chr13:79,477,364...79,481,231
JBrowse link
G NEK3 NIMA related kinase 3 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,132,647...52,159,597
Ensembl chr13:52,132,639...52,159,861
JBrowse link
G NEK5 NIMA related kinase 5 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,033,611...52,129,073
Ensembl chr13:52,033,611...52,129,092
JBrowse link
G NUDT15 nudix hydrolase 15 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:48,037,726...48,052,755
Ensembl chr13:48,037,726...48,047,221
JBrowse link
G OBI1 ORC ubiquitin ligase 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:78,614,286...78,659,165
Ensembl chr13:78,614,289...78,659,155
JBrowse link
G OBI1-AS1 OBI1 antisense RNA 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:78,054,855...78,617,325
Ensembl chr13:77,919,689...78,617,328
JBrowse link
G OLFM4 olfactomedin 4 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:53,028,813...53,052,057
Ensembl chr13:53,028,813...53,052,057
JBrowse link
G OR7E104P olfactory receptor family 7 subfamily E member 104 pseudogene IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:63,828,840...63,844,125
Ensembl chr13:63,828,840...63,844,125
JBrowse link
G PCDH17 protocadherin 17 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:57,630,104...57,729,311
Ensembl chr13:57,631,744...57,729,311
JBrowse link
G PCDH20 protocadherin 20 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:61,409,685...61,415,522
Ensembl chr13:61,409,685...61,415,522
JBrowse link
G PCDH8 protocadherin 8 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,842,889...52,848,640
Ensembl chr13:52,842,889...52,848,641
JBrowse link
G PCDH9 protocadherin 9 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:66,302,834...67,230,336
Ensembl chr13:66,302,834...67,230,445
JBrowse link
G PCDH9-AS2 PCDH9 antisense RNA 2 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:66,825,169...66,915,031
Ensembl chr13:66,825,169...66,915,031
JBrowse link
G PCDH9-AS3 PCDH9 antisense RNA 3 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:66,977,389...66,985,776
Ensembl chr13:66,977,432...66,985,776
JBrowse link
G PCDH9-AS4 PCDH9 antisense RNA 4 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:66,990,886...67,002,000
Ensembl chr13:66,990,886...67,002,007
JBrowse link
G PHF11 PHD finger protein 11 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,495,953...49,528,992
Ensembl chr13:49,495,610...49,528,981
JBrowse link
G PIBF1 progesterone immunomodulatory binding factor 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:72,782,133...73,016,461
Ensembl chr13:72,782,133...73,016,461
JBrowse link
G POU4F1 POU class 4 homeobox 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:78,598,362...78,603,552
Ensembl chr13:78,598,362...78,603,552
JBrowse link
G PRR20A proline rich 20A IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:57,140,918...57,143,939
Ensembl chr13:57,140,918...57,143,939
JBrowse link
G PRR20B proline rich 20B IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:57,147,488...57,150,509
Ensembl chr13:57,147,488...57,150,509
JBrowse link
G PRR20C proline rich 20C IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:57,154,061...57,157,082
Ensembl chr13:57,140,918...57,157,082
JBrowse link
G PRR20D proline rich 20D IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:57,160,632...57,163,653
Ensembl chr13:57,160,632...57,163,653
JBrowse link
G PRR20E proline rich 20E IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:57,167,197...57,170,218
Ensembl chr13:57,167,197...57,170,218
JBrowse link
G RB1 RB transcriptional corepressor 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:48,303,751...48,481,890
Ensembl chr13:48,303,744...48,599,436
Ensembl chr13:48,303,744...48,599,436
JBrowse link
G RB1-DT RB1 divergent transcript IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:48,296,513...48,303,702
Ensembl chr13:48,296,162...48,303,661
JBrowse link
G RBM26 RNA binding motif protein 26 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:79,311,827...79,406,255
Ensembl chr13:79,311,824...79,406,477
JBrowse link
G RBM26-AS1 RBM26 antisense RNA 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:79,406,309...79,424,336
Ensembl chr13:79,406,293...79,427,317
JBrowse link
G RCBTB1 RCC1 and BTB domain containing protein 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,531,944...49,585,587
Ensembl chr13:49,531,946...49,585,558
JBrowse link
G RCBTB2 RCC1 and BTB domain containing protein 2 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:48,488,963...48,535,997
Ensembl chr13:48,488,959...48,533,256
JBrowse link
G RNASEH2B ribonuclease H2 subunit B IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:50,909,678...50,970,462
Ensembl chr13:50,909,747...51,024,120
Ensembl chr13:50,909,747...51,024,120
JBrowse link
G RNASEH2B-AS1 RNASEH2B antisense RNA 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:50,882,378...50,910,712
Ensembl chr13:50,862,172...50,910,764
JBrowse link
G SCEL sciellin IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:77,535,694...77,645,263
Ensembl chr13:77,535,674...77,645,263
JBrowse link
G SCEL-AS1 SCEL antisense RNA 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:77,599,755...77,606,551
Ensembl chr13:77,599,755...77,606,551
JBrowse link
G SERPINE3 serpin family E member 3 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:51,335,804...51,365,454
Ensembl chr13:51,335,773...51,364,735
JBrowse link
G SETDB2 SET domain bifurcated histone lysine methyltransferase 2 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,444,274...49,495,003
Ensembl chr13:49,444,374...49,495,003
JBrowse link
G SETDB2-PHF11 SETDB2-PHF11 readthrough IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,444,274...49,528,976 JBrowse link
G SLAIN1 SLAIN motif family member 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:77,697,674...77,764,231
Ensembl chr13:77,697,687...77,764,242
JBrowse link
G SLITRK1 SLIT and NTRK like family member 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:83,877,205...83,882,474
Ensembl chr13:83,877,205...83,882,393
Ensembl chr13:83,877,205...83,882,393
JBrowse link
G SLITRK6 SLIT and NTRK like family member 6 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:85,792,790...85,799,419
Ensembl chr13:85,792,790...85,806,683
JBrowse link
G SNORA107 small nucleolar RNA, H/ACA box 107 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:84,783,654...84,783,778 JBrowse link
G SPRY2 sprouty RTK signaling antagonist 2 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:80,335,976...80,341,126
Ensembl chr13:80,335,976...80,341,126
JBrowse link
G SPRYD7 SPRY domain containing 7 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,912,702...49,936,501
Ensembl chr13:49,912,702...49,936,490
JBrowse link
G SUCLA2 succinate-CoA ligase ADP-forming subunit beta IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:47,942,656...48,001,273
Ensembl chr13:47,745,736...48,037,968
JBrowse link
G SUCLA2-AS1 SUCLA2 antisense RNA 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:48,001,389...48,002,614
Ensembl chr13:48,001,389...48,002,552
JBrowse link
G SUGT1 SGT1 homolog, MIS12 kinetochore complex assembly cochaperone IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,652,703...52,700,909
Ensembl chr13:52,652,709...52,700,909
JBrowse link
G TBC1D4 TBC1 domain family member 4 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:75,283,503...75,483,144
Ensembl chr13:75,283,503...75,482,169
JBrowse link
G TDRD3 tudor domain containing 3 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:60,396,457...60,573,879
Ensembl chr13:60,396,457...60,573,878
JBrowse link
G THSD1 thrombospondin type 1 domain containing 1 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,377,167...52,406,172
Ensembl chr13:52,377,167...52,416,373
JBrowse link
G TMEM272 transmembrane protein 272 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:51,813,347...51,845,177
Ensembl chr13:51,813,347...51,845,177
JBrowse link
G TRIM13 tripartite motif containing 13 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:49,997,042...50,018,467
Ensembl chr13:49,995,888...50,020,481
JBrowse link
G UCHL3 ubiquitin C-terminal hydrolase L3 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:75,549,490...75,606,020
Ensembl chr13:75,549,480...75,606,020
JBrowse link
G UTP14C UTP14C small subunit processome component IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,024,691...52,033,600
Ensembl chr13:52,024,691...52,033,600
JBrowse link
G VPS36 vacuolar protein sorting 36 homolog IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:52,412,606...52,450,634
Ensembl chr13:52,412,602...52,450,634
JBrowse link
G WDFY2 WD repeat and FYVE domain containing 2 IAGP ClinVar Annotator: match by term: Chromosome 13q14 deletion syndrome ClinVar NCBI chr13:51,584,194...51,767,709
Ensembl chr13:51,584,455...51,767,709
JBrowse link
conjunctival squamous cell carcinoma term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G ADAM3A ADAM metallopeptidase domain 3A (pseudogene) IAGP DNA, mRNA:amplification, increase expression RGD PMID:25491297 RGD:13831354 NCBI chr 8:39,451,045...39,522,989
Ensembl chr 8:39,451,045...39,522,852
JBrowse link
Distal Arthrogryposis, with Impaired Proprioception and Touch term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G PIEZO2 piezo type mechanosensitive ion channel component 2 IAGP ClinVar Annotator: match by term: Arthrogryposis, distal, with impaired proprioception and touch ClinVar
OMIM
PMID:25741868, PMID:27607563, PMID:27653382, PMID:27843126, PMID:27974811, PMID:28492532, PMID:31680123 NCBI chr18:10,670,237...11,149,585
Ensembl chr18:10,666,483...11,149,569
Ensembl chr18:10,666,483...11,149,569
JBrowse link
familial retinoblastoma term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G RB1 RB transcriptional corepressor 1 IAGP DNA:mutations:promoter, intron, exon:multiple RGD PMID:17096365 RGD:8547984 NCBI chr13:48,303,751...48,481,890
Ensembl chr13:48,303,744...48,599,436
Ensembl chr13:48,303,744...48,599,436
JBrowse link
Hyperalgesia term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G ABAT 4-aminobutyrate aminotransferase treatment ISO RGD PMID:24890317 RGD:9588557 NCBI chr16:8,674,617...8,784,575
Ensembl chr16:8,674,596...8,784,575
JBrowse link
G ADK adenosine kinase ISO associated with diabetic neuropathies; RGD PMID:11423084, PMID:9932716 RGD:6482662, RGD:6482666 NCBI chr10:74,151,185...74,709,300
Ensembl chr10:74,151,202...74,709,963
JBrowse link
G ADM adrenomedullin ISO
EXP
CTD Direct Evidence: marker/mechanism CTD PMID:17043245, PMID:17043245 RGD:1625316 NCBI chr11:10,305,073...10,307,397
Ensembl chr11:10,305,073...10,307,397
JBrowse link
G ADORA1 adenosine A1 receptor ISO associated with Spinal Cord Injuries RGD PMID:20065990 RGD:5129094 NCBI chr 1:203,127,705...203,167,405
Ensembl chr 1:203,090,654...203,167,405
JBrowse link
G ADRA1A adrenoceptor alpha 1A ISO associated with Diabetes Mellitus, Experimental; mRNA:increased expression:dorsal root ganglion RGD PMID:10841349 RGD:5688377 NCBI chr 8:26,738,113...26,870,994
Ensembl chr 8:26,748,150...26,867,278
JBrowse link
G ADRA2A adrenoceptor alpha 2A ISO RGD PMID:17959985 RGD:6480488 NCBI chr10:111,077,029...111,080,907
Ensembl chr10:111,077,029...111,080,907
JBrowse link
G ADRA2C adrenoceptor alpha 2C ISO RGD PMID:20007733 RGD:6893568 NCBI chr 4:3,766,385...3,768,526
Ensembl chr 4:3,766,348...3,768,526
JBrowse link
G ADRB1 adrenoceptor beta 1 ISO RGD PMID:19283893 RGD:5129125 NCBI chr10:114,043,866...114,046,904
Ensembl chr10:114,043,866...114,046,904
JBrowse link
G AGER advanced glycosylation end-product specific receptor treatment ISO
EXP
CTD Direct Evidence: marker/mechanism CTD PMID:25014009, PMID:25014009, PMID:24077211 RGD:8695980, RGD:7364865 NCBI chr 6:32,180,969...32,184,380
Ensembl chr 6:32,180,968...32,184,322
JBrowse link
G AGT angiotensinogen EXP CTD Direct Evidence: marker/mechanism CTD PMID:9613798 NCBI chr 1:230,702,523...230,745,583
Ensembl chr 1:230,702,523...230,714,122
JBrowse link
G AIF1 allograft inflammatory factor 1 ISO
EXP
associated with Alcohol-Induced Disorders, Nervous System; protein:increased expression:spinal cord (rat)
CTD Direct Evidence: marker/mechanism
CTD PMID:27093858, PMID:17284346 RGD:2313035 NCBI chr 6:31,615,212...31,617,015
Ensembl chr 6:31,615,217...31,617,021
JBrowse link
G AKR1B1 aldo-keto reductase family 1 member B ISO associated with Hyperglycemia RGD PMID:12505670 RGD:1626082 NCBI chr 7:134,442,350...134,459,239
Ensembl chr 7:134,442,356...134,459,284
JBrowse link
G ALOX12 arachidonate 12-lipoxygenase, 12S type EXP CTD Direct Evidence: marker/mechanism CTD PMID:12582831 NCBI chr17:6,993,791...7,010,754
Ensembl chr17:6,996,049...7,010,754
JBrowse link
G ALOX5 arachidonate 5-lipoxygenase EXP CTD Direct Evidence: marker/mechanism CTD PMID:12582831 NCBI chr10:45,374,209...45,446,121
Ensembl chr10:45,374,176...45,446,119
JBrowse link
G ANO3 anoctamin 3 ISO RGD PMID:23872594 RGD:9681745 NCBI chr11:26,188,808...26,667,907
Ensembl chr11:26,188,842...26,663,289
JBrowse link
G ANXA1 annexin A1 ISO protein:increased expression:dorsal root ganglion RGD PMID:9222544, PMID:21990306 RGD:2306950, RGD:7421656 NCBI chr 9:73,151,865...73,170,393
Ensembl chr 9:73,151,865...73,170,393
JBrowse link
G AQP4 aquaporin 4 ISO associated with Spinal Cord Injuries;mRNA,protein:increased expression:brain,spinal cord: RGD PMID:16219025 RGD:8695957 NCBI chr18:26,852,038...26,865,803
Ensembl chr18:26,852,043...26,865,771
JBrowse link
G AVP arginine vasopressin EXP CTD Direct Evidence: marker/mechanism CTD PMID:9613798 NCBI chr20:3,082,556...3,093,521
Ensembl chr20:3,082,556...3,084,724
JBrowse link
G BACE1 beta-secretase 1 ISO RGD PMID:28012171 RGD:13782150 NCBI chr11:117,285,207...117,316,256
Ensembl chr11:117,285,207...117,316,259
JBrowse link
G BDKRB1 bradykinin receptor B1 ISO
EXP
CTD Direct Evidence: marker/mechanism CTD PMID:17989505, PMID:19300402, PMID:19815945, PMID:12927641, PMID:12637034 RGD:1579989, RGD:7241581 NCBI chr14:96,256,210...96,264,763
Ensembl chr14:96,256,210...96,268,967
JBrowse link
G BDKRB2 bradykinin receptor B2 ISO
EXP
CTD Direct Evidence: marker/mechanism
associated with Diabetic Neuropathy
CTD PMID:17989505, PMID:19300402, PMID:19815945, PMID:10188975, PMID:19300402 RGD:4891040, RGD:2313332 NCBI chr14:96,204,839...96,244,164
Ensembl chr14:96,204,679...96,244,166
JBrowse link
G BDNF brain derived neurotrophic factor ISO
IDA
associated with Peripheral Nerve Injuries;
associated with inflammation;protein:increased expression:dorsal root ganglion:
associated with Sciatic Neuropathy;
associated with Pancreatitis, Chronic;
RGD PMID:11425916, PMID:21958434, PMID:10779676, PMID:12435470, PMID:21864655, PMID:21499209, PMID:12470870 RGD:8657088, RGD:8657122, RGD:8657114, RGD:8657101, RGD:8657099, RGD:8657093, RGD:8657091 NCBI chr11:27,654,893...27,722,030
Ensembl chr11:27,654,893...27,722,058
JBrowse link
G BECN1 beclin 1 ISO RGD PMID:23665054 RGD:11560531 NCBI chr17:42,810,132...42,824,282
Ensembl chr17:42,810,134...42,833,350
JBrowse link
G C3 complement C3 ISO associated with Sciatic Neuropathy;mRNA, protein:increased expression:spinal cord RGD PMID:23588254 RGD:7401259 NCBI chr19:6,677,704...6,720,650
Ensembl chr19:6,677,704...6,730,562
JBrowse link
G CACNA1B calcium voltage-gated channel subunit alpha1 B ISO RGD PMID:17567797 RGD:1626313 NCBI chr 9:137,877,782...138,124,619
Ensembl chr 9:137,877,782...138,124,624
JBrowse link
G CACNA1H calcium voltage-gated channel subunit alpha1 H EXP CTD Direct Evidence: marker/mechanism CTD PMID:19577366, PMID:30552955 NCBI chr16:1,153,106...1,221,769
Ensembl chr16:1,153,106...1,221,771
JBrowse link
G CACNA1I calcium voltage-gated channel subunit alpha1 I ISO RGD PMID:17112407 RGD:15003199 NCBI chr22:39,570,753...39,689,737
Ensembl chr22:39,570,753...39,689,735
JBrowse link
G CACNA2D1 calcium voltage-gated channel auxiliary subunit alpha2delta 1 EXP CTD Direct Evidence: marker/mechanism CTD PMID:11245671, PMID:17881535, PMID:24133248 NCBI chr 7:81,946,444...82,443,956
Ensembl chr 7:81,946,444...82,443,777
JBrowse link
G CALCA calcitonin related polypeptide alpha ISO
EXP
associated with inflammation;protein:increased expression:dorsal root ganglion:
CTD Direct Evidence: marker/mechanism|therapeutic
CTD PMID:12787826, PMID:12855330, PMID:15265675, PMID:27093858, PMID:21958434 RGD:8657122 NCBI chr11:14,966,668...14,972,361
Ensembl chr11:14,966,668...14,972,354
JBrowse link
G CAMK2A calcium/calmodulin dependent protein kinase II alpha EXP
ISO
CTD Direct Evidence: marker/mechanism CTD PMID:20053885, PMID:18042863 RGD:7240711 NCBI chr 5:150,219,491...150,290,130
Ensembl chr 5:150,219,491...150,290,291
JBrowse link
G CAPN2 calpain 2 treatment ISO associated with Peripheral Nerve Injuries RGD PMID:25150005 RGD:13792585 NCBI chr 1:223,701,597...223,776,018
Ensembl chr 1:223,701,593...223,776,018
JBrowse link
G CARTPT CART prepropeptide EXP CTD Direct Evidence: therapeutic CTD PMID:21167239 NCBI chr 5:71,719,275...71,721,045
Ensembl chr 5:71,719,275...71,721,048
JBrowse link
G CAT catalase treatment ISO RGD PMID:23952340, PMID:23658840 RGD:9479063, RGD:9479069 NCBI chr11:34,438,934...34,472,060
Ensembl chr11:34,438,934...34,472,060
JBrowse link
G CCK cholecystokinin ISO RGD PMID:15647484 RGD:1626108 NCBI chr 3:42,257,826...42,266,185
Ensembl chr 3:42,257,825...42,266,185
JBrowse link
G CCKBR cholecystokinin B receptor ISO
EXP
CTD Direct Evidence: marker/mechanism CTD PMID:11880531, PMID:15647484 RGD:1626108 NCBI chr11:6,259,838...6,272,127
Ensembl chr11:6,259,806...6,272,127
JBrowse link
G CCL2 C-C motif chemokine ligand 2 ISO
EXP
CTD Direct Evidence: marker/mechanism
protein:increased expression:dorsal root ganglion, spinal cord (rat)
CTD PMID:17881535, PMID:18419759, PMID:21712071, PMID:20737477, PMID:22531750 RGD:2307043, RGD:8548873, RGD:8548848, RGD:8548845 NCBI chr17:34,255,285...34,257,203
Ensembl chr17:34,255,218...34,257,203
JBrowse link
G CCL5 C-C motif chemokine ligand 5 ISO mRNA:increased expression:dorsal root ganglion (rat) RGD PMID:18076762, PMID:18656466 RGD:4890034, RGD:2303121 NCBI chr17:35,871,491...35,880,360
Ensembl chr17:35,871,491...35,880,793
JBrowse link
G CCR2 C-C motif chemokine receptor 2 ISO associated with Intervertebral disc disease;
associated with Demyelinating Diseases;
associated with Sciatic Neuropathy;
protein:increased expression:dorsal horn of spinal cord:
associated with Bone Neoplasms;protein:increased expression:spinal cord:
RGD PMID:18419759, PMID:24462503, PMID:18076762, PMID:24907405, PMID:22721162, PMID:23511129 RGD:2307043, RGD:8661788, RGD:4890034, RGD:8661781, RGD:8548831, RGD:8661772 NCBI chr 3:46,354,111...46,360,940
Ensembl chr 3:46,353,744...46,360,940
Ensembl chr 3:46,353,744...46,360,940
JBrowse link
G CCR5 C-C motif chemokine receptor 5 ISO mRNA:increased expression:dorsal root ganglion (rat)
associated with Spinal Cord Injuries
RGD PMID:18076762, PMID:22033364, PMID:23147416, PMID:24589480 RGD:4890034, RGD:8551820, RGD:8551809, RGD:8551795 NCBI chr 3:46,370,142...46,376,206
Ensembl chr 3:46,370,854...46,376,206
JBrowse link
G CFL1 cofilin 1 ISO protein:increased phosphorylation:dorsal root ganglion (rat) RGD PMID:24962708 RGD:11570412 NCBI chr11:65,854,673...65,858,180
Ensembl chr11:65,823,022...65,862,026
JBrowse link
G CNR1 cannabinoid receptor 1 EXP CTD Direct Evidence: therapeutic CTD PMID:17572696 NCBI chr 6:88,139,864...88,167,349
Ensembl chr 6:88,139,864...88,166,359
JBrowse link
G CNR2 cannabinoid receptor 2 EXP CTD Direct Evidence: marker/mechanism|therapeutic CTD PMID:17572696, PMID:18664590 NCBI chr 1:23,870,515...23,913,362
Ensembl chr 1:23,870,515...23,913,362
JBrowse link
G COMT catechol-O-methyltransferase ISO
EXP
CTD Direct Evidence: marker/mechanism CTD PMID:28195063, PMID:20726980 RGD:8662326 NCBI chr22:19,941,772...19,969,975
Ensembl chr22:19,941,733...19,969,975
Ensembl chr22:19,941,733...19,969,975
JBrowse link
G CRCP CGRP receptor component ISO RGD PMID:12895509 RGD:727768 NCBI chr 7:66,114,818...66,154,568
Ensembl chr 7:66,114,604...66,154,568
JBrowse link
G CRHR1 corticotropin releasing hormone receptor 1 EXP CTD Direct Evidence: marker/mechanism CTD PMID:28434951 NCBI chr17:45,784,320...45,835,828
Ensembl chr17:45,784,280...45,835,828
JBrowse link
G CSF3 colony stimulating factor 3 treatment IDA associated with Sciatic Neuropathy; RGD PMID:24253780 RGD:11039470 NCBI chr17:40,015,440...40,017,813
Ensembl chr17:40,015,361...40,017,813
JBrowse link
G CSK C-terminal Src kinase EXP CTD Direct Evidence: marker/mechanism CTD PMID:16769263 NCBI chr15:74,782,080...74,803,198
Ensembl chr15:74,782,057...74,803,198
JBrowse link
G CTSS cathepsin S ISO associated with Arthritis, Experimental
associated with Colitis
RGD PMID:22213084, PMID:21802389 RGD:5686870, RGD:5686873 NCBI chr 1:150,730,188...150,765,778
Ensembl chr 1:150,730,188...150,765,792
JBrowse link
G CX3CL1 C-X3-C motif chemokine ligand 1 treatment ISO associated with Arthritis, Experimental RGD PMID:19249394, PMID:22647647 RGD:2304251, RGD:9491779 NCBI chr16:57,372,490...57,385,044
Ensembl chr16:57,372,477...57,385,044
JBrowse link
G CX3CR1 C-X3-C motif chemokine receptor 1 ISO associated with Sciatic Neuropathy
associated with Arthritis, Experimental;protein:increased expression:lumbar spinal cord
associated with Inflammation
associated with Bone Neoplasms
RGD PMID:19959384, PMID:22647647, PMID:16324111, PMID:20524966, PMID:20609517, PMID:20736819 RGD:4891942, RGD:9491779, RGD:9387859, RGD:9354422, RGD:4891885, RGD:4892020 NCBI chr 3:39,263,494...39,281,735
Ensembl chr 3:39,263,494...39,281,735
Ensembl chr 3:39,263,494...39,281,735
JBrowse link
G CXCL12 C-X-C motif chemokine ligand 12 ISO RGD PMID:28638088 RGD:13838657 NCBI chr10:44,292,088...44,385,097
Ensembl chr10:44,370,165...44,386,493
JBrowse link
G CXCL8 C-X-C motif chemokine ligand 8 EXP CTD Direct Evidence: marker/mechanism CTD PMID:7881729, PMID:10401557 NCBI chr 4:73,740,569...73,743,716
Ensembl chr 4:73,740,541...73,743,716
JBrowse link
G CXCR2 C-X-C motif chemokine receptor 2 ISO RGD PMID:19283893 RGD:5129125 NCBI chr 2:218,125,294...218,137,253
Ensembl chr 2:218,125,289...218,137,251
JBrowse link
G CXCR4 C-X-C motif chemokine receptor 4 treatment ISO RGD PMID:28638088, PMID:30142543 RGD:13838657, RGD:13838658 NCBI chr 2:136,114,349...136,118,149
Ensembl chr 2:136,114,349...136,118,149
Ensembl chr 2:136,114,349...136,118,149
JBrowse link
G CYBB cytochrome b-245 beta chain ISO associated with Spinal Cord Injuries; RGD PMID:20679217 RGD:11040629 NCBI chr  X:37,780,059...37,813,461
Ensembl chr  X:37,780,059...37,813,461
Ensembl chr  X:37,780,059...37,813,461
JBrowse link
G DLG4 discs large MAGUK scaffold protein 4 ISO associated with Diabetic Neuropathies: RGD PMID:20531396 RGD:7257680 NCBI chr17:7,187,187...7,220,050
Ensembl chr17:7,189,890...7,219,841
Ensembl chr17:7,189,890...7,219,841
Ensembl chr17:7,189,890...7,219,841
JBrowse link
G DNMT1 DNA methyltransferase 1 ISO RGD PMID:21682946 RGD:9588311 NCBI chr19:10,133,346...10,194,953
Ensembl chr19:10,133,345...10,231,286
JBrowse link
G DRD3 dopamine receptor D3 EXP CTD Direct Evidence: marker/mechanism CTD PMID:20433900 NCBI chr 3:114,127,580...114,199,407
Ensembl chr 3:114,127,580...114,199,407
Ensembl chr 3:114,127,580...114,199,407
JBrowse link
G DUSP1 dual specificity phosphatase 1 treatment ISO associated with Sciatic Neuropathy RGD PMID:22901764, PMID:22540262 RGD:7771531, RGD:7771574 NCBI chr 5:172,768,096...172,771,195
Ensembl chr 5:172,768,096...172,771,195
JBrowse link
G DUSP6 dual specificity phosphatase 6 treatment ISO associated with Sciatic Neuropathy RGD PMID:22901764 RGD:7771531 NCBI chr12:89,347,235...89,352,501
Ensembl chr12:89,347,235...89,352,501
JBrowse link
G EDN1 endothelin 1 susceptibility ISO
EXP
mRNA:increased expression:paw skin (mouse)
CTD Direct Evidence: marker/mechanism
CTD PMID:19429182, PMID:23347081, PMID:15664691 RGD:8661716, RGD:8661735 NCBI chr 6:12,256,463...12,297,194
Ensembl chr 6:12,290,361...12,297,194
JBrowse link
G ENPP2 ectonucleotide pyrophosphatase/phosphodiesterase 2 treatment ISO RGD PMID:20392816 RGD:9685429 NCBI chr 8:119,557,085...119,673,404
Ensembl chr 8:119,557,086...119,673,453
JBrowse link
G EP300 E1A binding protein p300 ISO RGD PMID:25263804 RGD:9588307 NCBI chr22:41,092,592...41,180,077
Ensembl chr22:41,092,592...41,180,077
JBrowse link
G EPHA4 EPH receptor A4 ISO associated with spinal cord injuries; RGD PMID:16959251 RGD:5688783 NCBI chr 2:221,418,027...221,574,202
Ensembl chr 2:221,418,027...221,574,202
JBrowse link
G EPHX2 epoxide hydrolase 2 ISO RGD PMID:16962614 RGD:5688387 NCBI chr 8:27,491,143...27,597,559
Ensembl chr 8:27,490,781...27,545,564
JBrowse link
G ESR1 estrogen receptor 1 ISO RGD PMID:19285805 RGD:8553066 NCBI chr 6:151,654,148...152,129,619
Ensembl chr 6:151,656,691...152,129,619
JBrowse link
G ESR2 estrogen receptor 2 ISO RGD PMID:17056036, PMID:19285805 RGD:5508846, RGD:8553066 NCBI chr14:64,226,707...64,338,631
Ensembl chr14:64,084,232...64,338,112
JBrowse link
G F2 coagulation factor II, thrombin ISO associated with Sciatic Neuropathy RGD PMID:16251448 RGD:7387272 NCBI chr11:46,719,213...46,739,506
Ensembl chr11:46,719,196...46,739,506
Ensembl chr11:46,719,196...46,739,506
JBrowse link
G F2R coagulation factor II thrombin receptor severity ISO RGD PMID:19674841, PMID:11877315, PMID:12717003 RGD:7387269, RGD:7387271, RGD:7387270 NCBI chr 5:76,716,126...76,735,770
Ensembl chr 5:76,716,126...76,735,770
JBrowse link
G FOS Fos proto-oncogene, AP-1 transcription factor subunit ISO
EXP
protein:increased expression:dorsal horn of spinal cord, neuron
CTD Direct Evidence: marker/mechanism
CTD PMID:27093858, PMID:22160634 RGD:9999169 NCBI chr14:75,278,828...75,282,230
Ensembl chr14:75,278,826...75,282,230
JBrowse link
G GAL galanin and GMAP prepropeptide EXP CTD Direct Evidence: marker/mechanism CTD PMID:12787826 NCBI chr11:68,684,544...68,691,175
Ensembl chr11:68,683,779...68,691,175
JBrowse link
G GDNF glial cell derived neurotrophic factor EXP CTD Direct Evidence: marker/mechanism CTD PMID:20457222 NCBI chr 5:37,812,677...37,840,044
Ensembl chr 5:37,812,677...37,840,041
JBrowse link
G GFAP glial fibrillary acidic protein ISO
EXP
associated with Spinal Cord Injuries;mRNA,protein:increased expression:brain,spinal cord:
CTD Direct Evidence: marker/mechanism
CTD PMID:27093858, PMID:16219025 RGD:8695957 NCBI chr17:44,903,159...44,915,552
Ensembl chr17:44,903,159...44,916,937
JBrowse link
G GFRA1 GDNF family receptor alpha 1 ISO RGD PMID:16464682 RGD:6218969 NCBI chr10:116,056,925...116,274,705
Ensembl chr10:116,056,925...116,273,467
JBrowse link
G GJA1 gap junction protein alpha 1 treatment ISO associated with Sciatic Neuropathy RGD PMID:24631560, PMID:23374942 RGD:8662447, RGD:8662456 NCBI chr 6:121,435,646...121,449,727
Ensembl chr 6:121,435,595...121,449,727
JBrowse link
G GRIN1 glutamate ionotropic receptor NMDA type subunit 1 EXP CTD Direct Evidence: marker/mechanism CTD PMID:27093858 NCBI chr 9:137,139,092...137,168,759
Ensembl chr 9:137,139,154...137,168,756
JBrowse link
G GRIN2A glutamate ionotropic receptor NMDA type subunit 2A ISO RGD PMID:29758384 RGD:13792698 NCBI chr16:9,753,404...10,182,928
Ensembl chr16:9,753,404...10,182,928
Ensembl chr16:9,753,404...10,182,928
JBrowse link
G GRIN2B glutamate ionotropic receptor NMDA type subunit 2B treatment ISO
EXP
CTD Direct Evidence: marker/mechanism CTD PMID:20042082, PMID:24204988 RGD:13210755 NCBI chr12:13,537,337...13,982,012
Ensembl chr12:13,437,942...13,982,002
Ensembl chr12:13,437,942...13,982,002
JBrowse link
G GRK2 G protein-coupled receptor kinase 2 treatment
severity
ISO associated with bone cancer
associated with Complex Regional Pain Syndromes
RGD PMID:26935064, PMID:22796071, PMID:25466829, PMID:26064176 RGD:13513996, RGD:13792780, RGD:13514049, RGD:13514046 NCBI chr11:67,266,420...67,286,556
Ensembl chr11:67,266,473...67,286,556
JBrowse link
G GRM8 glutamate metabotropic receptor 8 ISO RGD PMID:17113112 RGD:6771186 NCBI chr 7:126,438,598...127,252,941
Ensembl chr 7:126,438,598...127,253,093
Ensembl chr 7:126,438,598...127,253,093
JBrowse link
G HIF1A hypoxia inducible factor 1 subunit alpha ISO associated with Limb Ischemia;protein:increased expression:foot muscle, plantar RGD PMID:18691814 RGD:9068903 NCBI chr14:61,695,513...61,748,259
Ensembl chr14:61,695,513...61,748,259
JBrowse link
G HMGB1 high mobility group box 1 treatment ISO
EXP
CTD Direct Evidence: marker/mechanism CTD PMID:27474498, PMID:24077211, PMID:30142543 RGD:7364865, RGD:13838658 NCBI chr13:30,456,704...30,617,597
Ensembl chr13:30,456,704...30,617,597
JBrowse link
G HOXD1 homeobox D1 EXP CTD Direct Evidence: marker/mechanism CTD PMID:21151121 NCBI chr 2:176,188,668...176,190,907
Ensembl chr 2:176,188,668...176,190,907
JBrowse link
G HTR2A 5-hydroxytryptamine receptor 2A ISO
EXP
associated with Diabetic neuropathies;
CTD Direct Evidence: marker/mechanism
CTD PMID:17888573, PMID:18930597, PMID:20531396 RGD:7257680 NCBI chr13:46,831,546...46,898,082
Ensembl chr13:46,831,550...46,897,076
JBrowse link
G HTR7 5-hydroxytryptamine receptor 7 ISO RGD PMID:21693130, PMID:21843960 RGD:6480665, RGD:6482179 NCBI chr10:90,738,693...90,858,039
Ensembl chr10:90,740,823...90,858,039
JBrowse link
G IGF1 insulin like growth factor 1 EXP CTD Direct Evidence: therapeutic CTD PMID:9452187 NCBI chr12:102,395,860...102,481,839
Ensembl chr12:102,395,874...102,481,744
JBrowse link
G IL10 interleukin 10 treatment ISO
EXP
IMP
associated with Sciatic Neuropathy
CTD Direct Evidence: marker/mechanism|therapeutic
CTD PMID:7582491, PMID:17174526, PMID:23957449, PMID:24077211, PMID:22820166 RGD:7364792, RGD:7364865, RGD:7364827 NCBI chr 1:206,767,602...206,772,494
Ensembl chr 1:206,767,602...206,774,541
JBrowse link
G IL13 interleukin 13 treatment IDA RGD PMID:11399514 RGD:8549555 NCBI chr 5:132,656,522...132,661,110
Ensembl chr 5:132,656,263...132,661,110
JBrowse link
G IL17A interleukin 17A treatment ISO RGD PMID:23192794, PMID:23246025 RGD:9068942, RGD:9222699 NCBI chr 6:52,186,375...52,190,638
Ensembl chr 6:52,186,375...52,190,638
JBrowse link
G IL18 interleukin 18 treatment ISO associated with Peripheral Nerve Injuries RGD PMID:19036970 RGD:8655929 NCBI chr11:112,143,251...112,164,104
Ensembl chr11:112,143,253...112,164,096
JBrowse link
G IL1A interleukin 1 alpha EXP CTD Direct Evidence: marker/mechanism CTD PMID:12727271 NCBI chr 2:112,773,925...112,784,493
Ensembl chr 2:112,773,925...112,784,493
Ensembl chr 2:112,773,925...112,784,493
JBrowse link
G IL1B interleukin 1 beta ISO
EXP
IDA
CTD Direct Evidence: marker/mechanism
associated with Peripheral Nerve Injuries
CTD PMID:7582491, PMID:10401557, PMID:12727271, PMID:17320857, PMID:20937348, PMID:27093858, PMID:15317861, PMID:8741165, PMID:23159984, PMID:22265659 RGD:1626676, RGD:7401209, RGD:7175548, RGD:6482671 NCBI chr 2:112,829,751...112,836,843
Ensembl chr 2:112,829,751...112,836,816
JBrowse link
G IL1R1 interleukin 1 receptor type 1 ISO RGD PMID:19022353, PMID:11585580 RGD:8662898, RGD:8662903 NCBI chr 2:102,069,638...102,179,874
Ensembl chr 2:102,064,544...102,179,874
JBrowse link
G IL1RN interleukin 1 receptor antagonist severity
treatment
ISO
EXP
IDA
CTD Direct Evidence: marker/mechanism|therapeutic
associated with Arthritis, Experimental; rat model treated with human protein
CTD PMID:8864563, PMID:15317861, PMID:17174526, PMID:20937348, PMID:23092240, PMID:10903985, PMID:17959986, PMID:22933159 RGD:6909165, RGD:8549800, RGD:7401210, RGD:6909175 NCBI chr 2:113,099,365...113,134,016
Ensembl chr 2:113,107,214...113,134,016
JBrowse link
G IL2 interleukin 2 treatment ISO associated with Sciatic Neuropathy; mRNA,protein:increased expression:spinal cord: RGD PMID:12755376, PMID:18423867, PMID:22189457 RGD:8662973, RGD:8662980, RGD:8662977 NCBI chr 4:122,451,470...122,456,725
Ensembl chr 4:122,451,470...122,456,725
JBrowse link
G IL33 interleukin 33 ISO RGD PMID:29329586 RGD:40400909 NCBI chr 9:6,214,591...6,257,983
Ensembl chr 9:6,215,786...6,257,983
JBrowse link
G IL6 interleukin 6 ISO
EXP
associated with Foot Injuries; protein:increased expression:serum:
CTD Direct Evidence: marker/mechanism
mRNA:increased expression:dorsal root ganglion
CTD PMID:7582491, PMID:10401557, PMID:18652822, PMID:18988309, PMID:23953943 RGD:8662979, RGD:10402830 NCBI chr 7:22,725,889...22,732,002
Ensembl chr 7:22,725,884...22,732,002
JBrowse link
G IL6R interleukin 6 receptor ISO mRNA:increased expression:dorsal root ganglion RGD PMID:23953943 RGD:10402830 NCBI chr 1:154,405,343...154,469,450
Ensembl chr 1:154,405,193...154,469,450
JBrowse link
G INSR insulin receptor treatment ISO
EXP
associated with Diabetic Neuropathies
CTD Direct Evidence: marker/mechanism
CTD PMID:18331706, PMID:23511693 RGD:10403050 NCBI chr19:7,112,257...7,294,414
Ensembl chr19:7,112,255...7,294,414
JBrowse link
G ITGA1 integrin subunit alpha 1 ISO RGD PMID:14984413, PMID:15836982 RGD:2302389, RGD:2302139 NCBI chr 5:52,787,916...52,959,209
Ensembl chr 5:52,787,916...52,959,209
JBrowse link
G ITGA2 integrin subunit alpha 2 EXP CTD Direct Evidence: marker/mechanism CTD PMID:18234883 NCBI chr 5:52,989,352...53,094,779
Ensembl chr 5:52,989,340...53,094,779
JBrowse link
G ITGA3 integrin subunit alpha 3 ISO RGD PMID:15836982, PMID:14984413 RGD:2302139, RGD:2302389 NCBI chr17:50,056,065...50,090,481
Ensembl chr17:50,055,968...50,090,481
JBrowse link
G ITGA5 integrin subunit alpha 5 ISO RGD PMID:15836982, PMID:14984413 RGD:2302139, RGD:2302389 NCBI chr12:54,395,261...54,419,266
Ensembl chr12:54,395,261...54,419,266
JBrowse link
G ITGB1 integrin subunit beta 1 ISO RGD PMID:15836982, PMID:14984413 RGD:2302139, RGD:2302389 NCBI chr10:32,900,318...32,958,230
Ensembl chr10:32,900,318...33,005,792
JBrowse link
G ITPR1 inositol 1,4,5-trisphosphate receptor type 1 ISO RGD PMID:25972297 RGD:13793383 NCBI chr 3:4,493,348...4,847,506
Ensembl chr 3:4,493,345...4,847,840
JBrowse link
G JAK2 Janus kinase 2 treatment ISO associated with Diabetic Neuropathies RGD PMID:18636982, PMID:23511693 RGD:6483031, RGD:10403050 NCBI chr 9:4,984,390...5,129,948
Ensembl chr 9:4,984,390...5,128,183
Ensembl chr 9:4,984,390...5,128,183
JBrowse link
G JAK3 Janus kinase 3 treatment ISO RGD PMID:21434883 RGD:11533942 NCBI chr19:17,824,782...17,848,071
Ensembl chr19:17,824,780...17,848,071
JBrowse link
G KCNC4 potassium voltage-gated channel subfamily C member 4 ISO RGD PMID:17855600 RGD:10411908 NCBI chr 1:110,210,314...110,282,649
Ensembl chr 1:110,210,314...110,283,100
Ensembl chr 1:110,210,314...110,283,100
JBrowse link
G KCNK2 potassium two pore domain channel subfamily K member 2 ISO RGD PMID:16675954 RGD:9831112 NCBI chr 1:215,002,920...215,237,093
Ensembl chr 1:215,005,775...215,237,090
Ensembl chr 1:215,005,775...215,237,090
JBrowse link
G KCNQ3 potassium voltage-gated channel subfamily Q member 3 ISO associated with Bone Neoplasms;protein:decreased expression:dorsal root ganglia (rat) RGD PMID:23352759 RGD:9686417 NCBI chr 8:132,120,858...132,481,095
Ensembl chr 8:132,120,859...132,481,095
JBrowse link
G KMO kynurenine 3-monooxygenase treatment ISO RGD PMID:26524415 RGD:13703043 NCBI chr 1:241,531,883...241,595,642
Ensembl chr 1:241,532,134...241,595,642
JBrowse link
G KNG1 kininogen 1 ISO
EXP
CTD Direct Evidence: marker/mechanism CTD PMID:2010815, PMID:2128375, PMID:3061568, PMID:7493622, PMID:7582491, PMID:7881729, PMID:9714424, PMID:9720808, PMID:10401557, PMID:10499367, PMID:10543429, PMID:15626726, PMID:16259764, PMID:16793879, PMID:18234883, PMID:21521205, PMID:20868656 RGD:11059894 NCBI chr 3:186,717,359...186,744,410
Ensembl chr 3:186,717,348...186,744,410
JBrowse link
G MAP1LC3A microtubule associated protein 1 light chain 3 alpha ISO RGD PMID:23665054 RGD:11560531 NCBI chr20:34,546,823...34,560,345
Ensembl chr20:34,546,854...34,560,345
JBrowse link
G MAP2K3 mitogen-activated protein kinase kinase 3 onset ISO RGD PMID:19427893 RGD:7495807 NCBI chr17:21,284,679...21,315,240
Ensembl chr17:21,284,672...21,315,232
JBrowse link
G MAPK1 mitogen-activated protein kinase 1 EXP CTD Direct Evidence: marker/mechanism CTD PMID:12941468, PMID:27093858 NCBI chr22:21,759,657...21,867,680
Ensembl chr22:21,754,500...21,867,680
Ensembl chr22:21,754,500...21,867,680
JBrowse link
G MAPK3 mitogen-activated protein kinase 3 EXP CTD Direct Evidence: marker/mechanism CTD PMID:12941468, PMID:27093858 NCBI chr16:30,114,105...30,123,309
Ensembl chr16:30,114,105...30,123,506
JBrowse link
G MAPK7 mitogen-activated protein kinase 7 EXP CTD Direct Evidence: marker/mechanism CTD PMID:17237256 NCBI chr17:19,377,721...19,383,544
Ensembl chr17:19,377,721...19,383,544
JBrowse link
G MAPK8 mitogen-activated protein kinase 8 EXP CTD Direct Evidence: marker/mechanism CTD PMID:27093858 NCBI chr10:48,306,673...48,439,360
Ensembl chr10:48,306,639...48,439,360
JBrowse link
G MAPK9 mitogen-activated protein kinase 9 EXP CTD Direct Evidence: marker/mechanism CTD PMID:27093858 NCBI chr 5:180,233,143...180,292,083
Ensembl chr 5:180,233,143...180,292,099
JBrowse link
G MC1R melanocortin 1 receptor EXP CTD Direct Evidence: marker/mechanism CTD PMID:19996949 NCBI chr16:89,918,862...89,920,972
Ensembl chr16:89,912,119...89,920,973
Ensembl chr16:89,912,119...89,920,973
JBrowse link
G MC4R melanocortin 4 receptor ISO protein:increased expression:dorsal root ganglia (rat) RGD PMID:20081244 RGD:6484233 NCBI chr18:60,371,062...60,372,775
Ensembl chr18:60,371,062...60,372,775
JBrowse link
G MEN1 menin 1 ISO associated with Sciatic Neuropathy;protein:increased expression:spinal cord dorsal horn (rat) RGD PMID:20369282 RGD:9589142 NCBI chr11:64,803,514...64,811,294
Ensembl chr11:64,803,510...64,811,294
JBrowse link
G MFN2 mitofusin 2 ISO
EXP
mRNA:decreased expression:spinal cord (rat)
CTD Direct Evidence: marker/mechanism
CTD PMID:28587902, PMID:28587902 RGD:12910704 NCBI chr 1:11,980,215...12,013,508
Ensembl chr 1:11,980,181...12,015,211
Ensembl chr 1:11,980,181...12,015,211
JBrowse link
G MIR15B microRNA 15b ISO RGD PMID:28012171 RGD:13782150 NCBI chr 3:160,404,588...160,404,685
Ensembl chr 3:160,404,588...160,404,685
JBrowse link
G MIR381 microRNA 381 treatment ISO RGD PMID:30142543 RGD:13838658 NCBI chr14:101,045,920...101,045,994
Ensembl chr14:101,045,920...101,045,994
JBrowse link
G MIR96 microRNA 96 treatment ISO associated with Sciatic Neuropathy RGD PMID:24234845 RGD:11553932 NCBI chr 7:129,774,692...129,774,769
Ensembl chr 7:129,774,692...129,774,769
JBrowse link
G MMP3 matrix metallopeptidase 3 ISO
EXP
CTD Direct Evidence: marker/mechanism CTD PMID:18754875, PMID:22056600 RGD:8693664 NCBI chr11:102,835,801...102,843,609
Ensembl chr11:102,835,801...102,843,609
JBrowse link
G MPZ myelin protein zero EXP CTD Direct Evidence: marker/mechanism CTD PMID:16676325 NCBI chr 1:161,303,594...161,309,969
Ensembl chr 1:161,304,735...161,309,968
Ensembl chr 1:161,304,735...161,309,968
JBrowse link
G MTOR mechanistic target of rapamycin kinase ISO RGD PMID:24382350 RGD:10040983 NCBI chr 1:11,106,535...11,273,497
Ensembl chr 1:11,106,535...11,262,551
JBrowse link
G NEFH neurofilament heavy treatment ISO RGD PMID:21071147 RGD:27226885 NCBI chr22:29,480,218...29,491,390
Ensembl chr22:29,480,218...29,491,390
JBrowse link
G NGF nerve growth factor treatment ISO
EXP
associated with Cystitis
CTD Direct Evidence: marker/mechanism
associated with Peripheral Nerve Injuries;
CTD PMID:20457222, PMID:16203088, PMID:11425916, PMID:22839415, PMID:18448607 RGD:7242799, RGD:8657088, RGD:7242849, RGD:7242803 NCBI chr 1:115,285,915...115,338,253
Ensembl chr 1:115,285,917...115,338,256
Ensembl chr 1:115,285,917...115,338,256
Ensembl chr 1:115,285,917...115,338,256
JBrowse link
G NGFR nerve growth factor receptor treatment ISO associated with Brachial Plexus Neuropathies RGD PMID:23324933 RGD:10413898 NCBI chr17:49,495,293...49,515,008
Ensembl chr17:49,495,293...49,515,008
JBrowse link
G NLGN2 neuroligin 2 ISO RGD PMID:23891900 RGD:9831150 NCBI chr17:7,405,492...7,419,860
Ensembl chr17:7,404,874...7,419,860
JBrowse link
G NOS1 nitric oxide synthase 1 ISO
EXP
CTD Direct Evidence: marker/mechanism CTD PMID:19300402, PMID:23909597 RGD:7257597 NCBI chr12:117,208,142...117,361,626
Ensembl chr12:117,208,142...117,452,170
JBrowse link
G NOS2 nitric oxide synthase 2 EXP CTD Direct Evidence: marker/mechanism CTD PMID:17989504, PMID:19300402 NCBI chr17:27,756,766...27,800,529
Ensembl chr17:27,756,766...27,800,529
JBrowse link
G NPY neuropeptide Y treatment ISO associated with Sciatic Neuropathy RGD PMID:19556004 RGD:10448929 NCBI chr 7:24,284,190...24,291,862
Ensembl chr 7:24,284,188...24,291,862
JBrowse link
G NRG1 neuregulin 1 ISO associated with Sciatic Neuropathy RGD PMID:22212401 RGD:10449019 NCBI chr 8:31,639,245...32,774,046
Ensembl chr 8:31,639,222...32,855,666
JBrowse link
G NTF3 neurotrophin 3 EXP CTD Direct Evidence: therapeutic CTD PMID:15659614 NCBI chr12:5,432,108...5,495,299
Ensembl chr12:5,432,108...5,521,536
JBrowse link
G NTRK1 neurotrophic receptor tyrosine kinase 1 ISO RGD PMID:17667845, PMID:20351485 RGD:5144120, RGD:5684352 NCBI chr 1:156,815,750...156,881,850
Ensembl chr 1:156,815,640...156,881,850
JBrowse link
G NTRK2 neurotrophic receptor tyrosine kinase 2 ISO associated with inflammation;protein:increased expression:dorsal root ganglion: RGD PMID:12470870, PMID:21958434 RGD:8657091, RGD:8657122 NCBI chr 9:84,668,458...85,027,070
Ensembl chr 9:84,668,551...85,027,070
JBrowse link
G NTSR1 neurotensin receptor 1 ISO RGD PMID:22396077 RGD:9743902 NCBI chr20:62,708,770...62,762,771
Ensembl chr20:62,708,836...62,762,771
JBrowse link
G OPRK1 opioid receptor kappa 1 treatment ISO associated with Diabetes Mellitus, Experimental; RGD PMID:16924480 RGD:9834947 NCBI chr 8:53,225,724...53,251,637
Ensembl chr 8:53,225,724...53,251,637
Ensembl chr 8:53,225,724...53,251,637
JBrowse link
G OPRL1 opioid related nociceptin receptor 1 ISO associated with Sciatic Neuropathy;mRNA:increased expression:spinal cord lumbar segment,dorsal root ganglion: RGD PMID:12106803 RGD:9835017 NCBI chr20:64,080,082...64,100,643
Ensembl chr20:64,080,082...64,100,643
JBrowse link
G OPRM1 opioid receptor mu 1 EXP CTD Direct Evidence: marker/mechanism CTD PMID:17996026 NCBI chr 6:154,010,496...154,246,867
Ensembl chr 6:154,010,496...154,246,867
JBrowse link
G P2RX2 purinergic receptor P2X 2 EXP CTD Direct Evidence: marker/mechanism CTD PMID:19383439 NCBI chr12:132,618,776...132,623,736
Ensembl chr12:132,618,776...132,622,388
JBrowse link
G P2RX3 purinergic receptor P2X 3 EXP CTD Direct Evidence: marker/mechanism CTD PMID:19383439 NCBI chr11:57,335,943...57,372,399
Ensembl chr11:57,338,352...57,372,396
JBrowse link
G P2RY12 purinergic receptor P2Y12 ISO RGD PMID:20398327, PMID:20136836 RGD:6480525, RGD:6480526 NCBI chr 3:151,336,843...151,384,753
Ensembl chr 3:151,337,380...151,384,812
Ensembl chr 3:151,337,380...151,384,812
JBrowse link
G PAWR pro-apoptotic WT1 regulator treatment ISO RGD PMID:17179954 RGD:9835416 NCBI chr12:79,584,879...79,691,097
Ensembl chr12:79,574,979...79,690,964
JBrowse link
G PDYN prodynorphin EXP CTD Direct Evidence: marker/mechanism CTD PMID:17670969 NCBI chr20:1,978,756...1,994,285
Ensembl chr20:1,978,757...1,994,285
JBrowse link
G PENK proenkephalin treatment IDA associated with Diabetes Mellitus, Experimental; RGD PMID:23235561 RGD:10003116 NCBI chr 8:56,440,957...56,446,641
Ensembl chr 8:56,436,674...56,446,671
JBrowse link
G PLA2G4A phospholipase A2 group IVA ISO RGD PMID:16203828 RGD:1642461 NCBI chr 1:186,828,949...186,988,981
Ensembl chr 1:186,828,949...186,988,981
JBrowse link
G PNOC prepronociceptin EXP CTD Direct Evidence: marker/mechanism CTD PMID:12665541, PMID:19231294 NCBI chr 8:28,316,979...28,343,355
Ensembl chr 8:28,316,986...28,343,355
JBrowse link
G PPP2CA protein phosphatase 2 catalytic subunit alpha ISO RGD PMID:26732138 RGD:11572421 NCBI chr 5:134,194,332...134,226,073
Ensembl chr 5:134,194,332...134,226,073
JBrowse link
G PRKCB protein kinase C beta ISO associated with inflammation;protein:increased activity:spinal cord RGD PMID:16360284 RGD:1625519 NCBI chr16:23,835,983...24,220,611
Ensembl chr16:23,835,983...24,220,611
JBrowse link
G PRKCE protein kinase C epsilon EXP CTD Direct Evidence: marker/mechanism CTD PMID:11738263, PMID:12582831, PMID:20457222 NCBI chr 2:45,651,315...46,187,990
Ensembl chr 2:45,651,345...46,187,990
JBrowse link
G PRKCG protein kinase C gamma treatment EXP
IEP
CTD Direct Evidence: marker/mechanism CTD PMID:19955894, PMID:27093858, PMID:12560106 RGD:28867224 NCBI chr19:53,882,197...53,907,652
Ensembl chr19:53,879,190...53,907,652
JBrowse link
G PRKCZ protein kinase C zeta EXP CTD Direct Evidence: marker/mechanism CTD PMID:27899695 NCBI chr 1:2,050,411...2,185,395
Ensembl chr 1:2,050,411...2,185,395
JBrowse link
G PRKG1 protein kinase cGMP-dependent 1 treatment ISO RGD PMID:14973199 RGD:7775058 NCBI chr10:50,990,888...52,298,350
Ensembl chr10:50,990,888...52,298,423
JBrowse link
G PROK2 prokineticin 2 EXP CTD Direct Evidence: marker/mechanism CTD PMID:16793879 NCBI chr 3:71,771,655...71,785,148
Ensembl chr 3:71,771,655...71,785,206
JBrowse link
G PROKR1 prokineticin receptor 1 EXP CTD Direct Evidence: marker/mechanism CTD PMID:16793879 NCBI chr 2:68,643,579...68,658,251
Ensembl chr 2:68,643,589...68,658,247
Ensembl chr 2:68,643,589...68,658,247
JBrowse link
G PTAFR platelet activating factor receptor treatment ISO RGD PMID:16925995 RGD:10041052 NCBI chr 1:28,147,166...28,193,856
Ensembl chr 1:28,147,166...28,193,936
JBrowse link
G PTGER1 prostaglandin E receptor 1 EXP CTD Direct Evidence: marker/mechanism CTD PMID:11375261 NCBI chr19:14,472,466...14,475,354
Ensembl chr19:14,472,466...14,475,354
JBrowse link
G PTGER3 prostaglandin E receptor 3 ISO protein:increased expression:lumbar spinal cord dorsal horn (rat) RGD PMID:17413918 RGD:5688169 NCBI chr 1:70,852,358...71,047,816
Ensembl chr 1:70,852,353...71,047,808
JBrowse link
G PTGER4 prostaglandin E receptor 4 treatment ISO RGD PMID:20423341 RGD:10003041 NCBI chr 5:40,679,915...40,740,936
Ensembl chr 5:40,679,915...40,693,735
JBrowse link
G PTGES3 prostaglandin E synthase 3 ISO RGD PMID:16192391 RGD:5688057 NCBI chr12:56,663,349...56,689,575
Ensembl chr12:56,663,341...56,688,408
JBrowse link
G PTGS1 prostaglandin-endoperoxide synthase 1 ISO
EXP
protein:increased expression:spinal cord
CTD Direct Evidence: marker/mechanism
CTD PMID:17989504, PMID:17413918 RGD:5688169 NCBI chr 9:122,369,906...122,395,703
Ensembl chr 9:122,370,530...122,395,703
JBrowse link
G PTGS2 prostaglandin-endoperoxide synthase 2 ISO
EXP
CTD Direct Evidence: marker/mechanism CTD PMID:17112505, PMID:17989504, PMID:15464832 RGD:5688224 NCBI chr 1:186,671,791...186,680,423
Ensembl chr 1:186,671,791...186,680,423
JBrowse link
G PTHLH parathyroid hormone like hormone EXP CTD Direct Evidence: marker/mechanism CTD PMID:16769263 NCBI chr12:27,958,084...27,972,864
Ensembl chr12:27,958,084...27,972,733
JBrowse link
G RAF1 Raf-1 proto-oncogene, serine/threonine kinase EXP CTD Direct Evidence: marker/mechanism CTD PMID:18976650 NCBI chr 3:12,583,601...12,664,117
Ensembl chr 3:12,583,601...12,664,226
JBrowse link
G RGS4 regulator of G protein signaling 4 treatment ISO associated with lesion of sciatic nerve RGD PMID:27641322 RGD:13524513 NCBI chr 1:163,068,871...163,076,802
Ensembl chr 1:163,068,775...163,076,802
JBrowse link
G SCN10A sodium voltage-gated channel alpha subunit 10 ISO
EXP
CTD Direct Evidence: marker/mechanism CTD PMID:16545521, PMID:19070548 RGD:6484253 NCBI chr 3:38,696,807...38,816,217
Ensembl chr 3:38,696,802...38,816,286
JBrowse link
G SCN11A sodium voltage-gated channel alpha subunit 11 EXP CTD Direct Evidence: marker/mechanism CTD PMID:23264124 NCBI chr 3:38,845,764...39,051,944
Ensembl chr 3:38,845,764...39,052,157
Ensembl chr 3:38,845,764...39,052,157
JBrowse link
G SIN3A SIN3 transcription regulator family member A ISO associated with Arthritis, Experimental;mRNA:decreased expression:spinal cord, neuron RGD PMID:17553988 RGD:9495916 NCBI chr15:75,369,379...75,455,819
Ensembl chr15:75,369,379...75,455,842
JBrowse link
G SLC12A5 solute carrier family 12 member 5 EXP CTD Direct Evidence: marker/mechanism CTD PMID:20086212 NCBI chr20:46,021,686...46,060,150
Ensembl chr20:46,021,690...46,060,152
Ensembl chr20:46,021,690...46,060,152
JBrowse link
G SLC17A8 solute carrier family 17 member 8 ISO protein:increased expression:dorsal horn of spinal cord, neuron RGD PMID:22160634 RGD:9999169 NCBI chr12:100,357,074...100,422,055
Ensembl chr12:100,357,074...100,422,055
JBrowse link
G SPARC secreted protein acidic and cysteine rich EXP CTD Direct Evidence: marker/mechanism CTD PMID:20714283 NCBI chr 5:151,661,096...151,686,915
Ensembl chr 5:151,661,096...151,686,975
JBrowse link
G STAT3 signal transducer and activator of transcription 3 treatment ISO RGD PMID:24098399 RGD:8694290 NCBI chr17:42,313,324...42,388,502
Ensembl chr17:42,313,324...42,388,482
Ensembl chr17:42,313,324...42,388,482
JBrowse link
G SYN2 synapsin II EXP CTD Direct Evidence: marker/mechanism CTD PMID:18701217 NCBI chr 3:12,004,366...12,192,032
Ensembl chr 3:12,004,388...12,192,032
JBrowse link
G TAC1 tachykinin precursor 1 EXP CTD Direct Evidence: marker/mechanism CTD PMID:8864563, PMID:9714424, PMID:10499367, PMID:12351280, PMID:12787826, PMID:15626726, PMID:16259764, PMID:18234883, PMID:19231294 NCBI chr 7:97,732,086...97,740,472
Ensembl chr 7:97,732,084...97,740,472
JBrowse link
G TACR1 tachykinin receptor 1 EXP CTD Direct Evidence: marker/mechanism CTD PMID:15964684, PMID:17123731 NCBI chr 2:75,046,463...75,199,520
Ensembl chr 2:75,046,463...75,199,520
JBrowse link
G TGFBR1 transforming growth factor beta receptor 1 ISO associated with Experimental Pancreatitis, Chronic RGD PMID:26645248 RGD:14995470 NCBI chr 9:99,104,038...99,154,192
Ensembl chr 9:99,104,038...99,154,192
JBrowse link
G THBD thrombomodulin treatment IDA
EXP
associated with Inflammation
CTD Direct Evidence: therapeutic
CTD PMID:27474498, PMID:24004409 RGD:11038687 NCBI chr20:23,045,633...23,049,672
Ensembl chr20:23,045,633...23,049,672
Ensembl chr20:23,045,633...23,049,672
JBrowse link
G TLR2 toll like receptor 2 ISO RGD PMID:17355971, PMID:24204973 RGD:8553059, RGD:8553185 NCBI chr 4:153,684,080...153,710,643
Ensembl chr 4:153,684,070...153,706,260
Ensembl chr 4:153,684,070...153,706,260
JBrowse link
G TLR4 toll like receptor 4 ISO
IDA
RGD PMID:20714435, PMID:24204973, PMID:15809417 RGD:4144070, RGD:8553185, RGD:7815040 NCBI chr 9:117,704,403...117,724,735
Ensembl chr 9:117,704,175...117,724,735
JBrowse link
G TNF tumor necrosis factor ISO
EXP
protein:increased expression:lumbar vertebra:
CTD Direct Evidence: marker/mechanism
associated with Diabetic Neuropathies;
mRNA,protein:increased expression:spinal cord:
CTD PMID:7582491, PMID:7881729, PMID:10401557, PMID:12727271, PMID:16472913, PMID:17320857, PMID:18463260, PMID:18582539, PMID:20383154, PMID:26141506, PMID:27093858, PMID:16675114, PMID:21104419, PMID:17304130, PMID:10825476, PMID:18790011, PMID:17459378 RGD:7387300, RGD:7401179, RGD:7394757, RGD:7394741, RGD:7394737, RGD:7387302 NCBI chr 6:31,575,565...31,578,336
Ensembl chr 6:31,575,565...31,578,336
JBrowse link
G TNFRSF11B TNF receptor superfamily member 11b EXP CTD Direct Evidence: therapeutic CTD PMID:16769263 NCBI chr 8:118,923,557...118,951,885
Ensembl chr 8:118,923,557...118,951,885
JBrowse link
G TNFRSF1A TNF receptor superfamily member 1A treatment ISO associated with Sciatic Neuropathy RGD PMID:12752784, PMID:22652595, PMID:21712071, PMID:24257399, PMID:20417692, PMID:21145890 RGD:5130913, RGD:8661750, RGD:8548873, RGD:8661737, RGD:8661726, RGD:5130939 NCBI chr12:6,328,771...6,342,076
Ensembl chr12:6,328,757...6,342,114
JBrowse link
G TNFRSF1B TNF receptor superfamily member 1B ISO associated with Sciatic Neuropathy RGD PMID:18463260, PMID:22652595 RGD:5130960, RGD:8661750 NCBI chr 1:12,166,948...12,209,222
Ensembl chr 1:12,166,991...12,209,228
JBrowse link
G TRPA1 transient receptor potential cation channel subfamily A member 1 ISO
EXP
associated with Peripheral Nerve Injuries;
CTD Direct Evidence: marker/mechanism
CTD PMID:18234885, PMID:21481532, PMID:23523557, PMID:18954467 RGD:10043618 NCBI chr 8:72,021,250...72,094,885
Ensembl chr 8:72,019,917...72,075,584
JBrowse link
G TRPC1 transient receptor potential cation channel subfamily C member 1 ISO associated with Inflammation RGD PMID:19439599 RGD:7247605 NCBI chr 3:142,724,034...142,807,888
Ensembl chr 3:142,724,034...142,807,888
JBrowse link
G TRPC6 transient receptor potential cation channel subfamily C member 6 ISO RGD PMID:19439599 RGD:7247605 NCBI chr11:101,451,470...101,584,007
Ensembl chr11:101,451,564...101,872,562
JBrowse link
G TRPV1 transient receptor potential cation channel subfamily V member 1 ISO
EXP
associated with inflammation;protein:increased expression:dorsal root ganglion:
CTD Direct Evidence: marker/mechanism
CTD PMID:12151517, PMID:18234885, PMID:18774343, PMID:23006841, PMID:21958434 RGD:8657122 NCBI chr17:3,565,446...3,609,411
Ensembl chr17:3,565,444...3,609,411
JBrowse link
G TRPV4 transient receptor potential cation channel subfamily V member 4 EXP CTD Direct Evidence: marker/mechanism CTD PMID:18234883 NCBI chr12:109,783,087...109,833,398
Ensembl chr12:109,783,087...109,833,406
Ensembl chr12:109,783,087...109,833,406
JBrowse link
G VIP vasoactive intestinal peptide EXP CTD Direct Evidence: marker/mechanism CTD PMID:12787826 NCBI chr 6:152,750,797...152,759,765
Ensembl chr 6:152,750,797...152,759,765
JBrowse link
Hyperesthesia term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G KNG1 kininogen 1 EXP CTD Direct Evidence: marker/mechanism CTD PMID:8190269 NCBI chr 3:186,717,359...186,744,410
Ensembl chr 3:186,717,348...186,744,410
JBrowse link
Hypesthesia term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G DARS2 aspartyl-tRNA synthetase 2, mitochondrial IAGP ClinVar Annotator: match by term: Hypoesthesia ClinVar PMID:17384640, PMID:19592391, PMID:22843165, PMID:23065766, PMID:23652419, PMID:24005482, PMID:24407472, PMID:25741868, PMID:30311386 NCBI chr 1:173,824,673...173,858,546
Ensembl chr 1:173,824,653...173,858,808
JBrowse link
G DMD dystrophin IAGP ClinVar Annotator: match by term: Hypoesthesia ClinVar PMID:23352160, PMID:23871722, PMID:26467025, PMID:26743743, PMID:26990548, PMID:28492532, PMID:30311386, PMID:30415094 NCBI chr  X:31,119,219...33,339,460
Ensembl chr  X:31,097,677...33,339,441
JBrowse link
G FIG4 FIG4 phosphoinositide 5-phosphatase IAGP ClinVar Annotator: match by term: Hypoesthesia ClinVar PMID:26467025, PMID:28492532, PMID:29650794, PMID:30311386 NCBI chr 6:109,691,296...109,825,431
Ensembl chr 6:109,690,609...109,878,098
Ensembl chr 6:109,690,609...109,878,098
Ensembl chr 6:109,690,609...109,878,098
JBrowse link
G GJB1 gap junction protein beta 1 IAGP ClinVar Annotator: match by term: Hypoesthesia ClinVar PMID:25741868, PMID:30311386 NCBI chr  X:71,215,239...71,225,516
Ensembl chr  X:71,212,811...71,225,516
Ensembl chr  X:71,212,811...71,225,516
JBrowse link
Hypoalgesia term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G AQP4 aquaporin 4 ISO RGD PMID:20851747 RGD:8696005 NCBI chr18:26,852,038...26,865,803
Ensembl chr18:26,852,043...26,865,771
JBrowse link
G HDAC4 histone deacetylase 4 ISO RGD PMID:19672313 RGD:9681457 NCBI chr 2:239,048,168...239,401,649
Ensembl chr 2:239,048,168...239,401,654
JBrowse link
ocular melanoma term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G GNA11 G protein subunit alpha 11 IAGP ClinVar Annotator: match by term: Intraocular melanoma ClinVar PMID:1328859, PMID:2549426, PMID:21083380, PMID:21444680, PMID:22733540, PMID:22808163, PMID:24141786, PMID:25157968, PMID:26619011 NCBI chr19:3,094,362...3,123,999
Ensembl chr19:3,094,362...3,123,999
JBrowse link
G GNAQ G protein subunit alpha q IAGP ClinVar Annotator: match by term: Intraocular melanoma ClinVar PMID:1328859, PMID:2549426, PMID:18719078, PMID:19078957, PMID:21083380, PMID:22253748, PMID:22653968, PMID:22733540, PMID:22808163, PMID:25157968 NCBI chr 9:77,716,097...78,031,811
Ensembl chr 9:77,716,097...78,031,811
JBrowse link
Paresthesia term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G CAPN3 calpain 3 IAGP ClinVar Annotator: match by term: Paresthesias ClinVar PMID:7720071, PMID:9266733, PMID:10330340, PMID:10679950, PMID:14578192, PMID:14981715, PMID:15351423, PMID:15689361, PMID:15725583, PMID:16100770, PMID:16141003, PMID:16650086, PMID:17318636, PMID:20635405, PMID:21204801, PMID:21984748, PMID:25741868, PMID:26467025, PMID:27142102, PMID:28492532, PMID:30311386 NCBI chr15:42,359,501...42,412,317
Ensembl chr15:42,359,498...42,412,949
Ensembl chr15:42,359,498...42,412,949
JBrowse link
G FKRP fukutin related protein IAGP ClinVar Annotator: match by term: Paresthesias ClinVar PMID:11741828, PMID:12666124, PMID:14647208, PMID:15060126, PMID:15574464, PMID:15580560, PMID:15833432, PMID:15886712, PMID:16634037, PMID:16786213, PMID:17554798, PMID:18060779, PMID:18593008, PMID:18639457, PMID:19820980, PMID:19835634, PMID:19900540, PMID:21220724, PMID:21228398, PMID:22264518, PMID:22981120, PMID:23576288, PMID:23591631, PMID:24033266, PMID:24447024, PMID:25048216, PMID:25560911, PMID:25741868, PMID:26363967, PMID:26467025, PMID:26574668, PMID:26833294, PMID:28492532, PMID:30311386 NCBI chr19:46,746,015...46,758,575
Ensembl chr19:46,746,046...46,776,988
JBrowse link
G INS insulin EXP CTD Direct Evidence: marker/mechanism CTD PMID:9861226 NCBI chr11:2,159,779...2,161,209
Ensembl chr11:2,159,779...2,161,341
Ensembl chr11:2,159,779...2,161,341
JBrowse link
G PMP22 peripheral myelin protein 22 EXP CTD Direct Evidence: marker/mechanism CTD PMID:12427913 NCBI chr17:15,229,779...15,265,326
Ensembl chr17:15,229,773...15,272,292
Ensembl chr17:15,229,773...15,272,292
JBrowse link
retinoblastoma term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G ALK ALK receptor tyrosine kinase IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:25741868, PMID:28492532 NCBI chr 2:29,190,992...29,921,589
Ensembl chr 2:29,192,774...29,921,586
JBrowse link
G APC APC regulator of WNT signaling pathway IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:25186627, PMID:25741868, PMID:28492532 NCBI chr 5:112,707,498...112,846,239
Ensembl chr 5:112,707,498...112,846,239
JBrowse link
G BRCA2 BRCA2 DNA repair associated IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:17899372, PMID:19043619, PMID:20507642, PMID:22632462, PMID:25741868, PMID:25782689, PMID:28492532, PMID:29394989, PMID:29884841, PMID:30254663 NCBI chr13:32,315,508...32,400,268
Ensembl chr13:32,315,086...32,400,268
Ensembl chr13:32,315,086...32,400,268
JBrowse link
G CADM2 cell adhesion molecule 2 IEP mRNA, protein:decreased expression:retina RGD PMID:30320366 RGD:15092072 NCBI chr 3:84,958,989...86,074,429
Ensembl chr 3:84,958,981...86,074,429
JBrowse link
G CDKN2A cyclin dependent kinase inhibitor 2A IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:25741868 NCBI chr 9:21,967,752...21,995,324
Ensembl chr 9:21,967,753...21,995,301
JBrowse link
G FANCM FA complementation group M IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:25741868 NCBI chr14:45,135,930...45,200,890
Ensembl chr14:45,135,930...45,200,890
JBrowse link
G FAS Fas cell surface death receptor severity IEP protein:decreased expression:tumor (human) RGD PMID:14533029 RGD:8662811 NCBI chr10:88,968,429...89,017,059
Ensembl chr10:88,990,531...89,017,059
JBrowse link
G ITM2B integral membrane protein 2B IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:8099255, PMID:12541220, PMID:28492532, PMID:28575107, PMID:29568217 NCBI chr13:48,233,206...48,270,357
Ensembl chr13:48,232,612...48,270,357
JBrowse link
G KDM1B lysine demethylase 1B IEP mRNA:increased expression:retina (human) RGD PMID:16180235 RGD:9588276 NCBI chr 6:18,155,388...18,223,854
Ensembl chr 6:18,155,329...18,223,854
JBrowse link
G LPAR6 lysophosphatidic acid receptor 6 IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:8099255, PMID:12541220, PMID:21505449, PMID:22909775, PMID:23301675, PMID:28492532, PMID:28575107, PMID:29568217 NCBI chr13:48,400,897...48,444,669
Ensembl chr13:48,389,567...48,444,704
JBrowse link
G MAX MYC associated factor X IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:25741868, PMID:28492532 NCBI chr14:65,006,101...65,102,695
Ensembl chr14:65,006,174...65,102,695
JBrowse link
G MED4 mediator complex subunit 4 IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:8099255, PMID:12541220, PMID:28492532, PMID:28575107, PMID:29568217 NCBI chr13:48,075,724...48,095,104
Ensembl chr13:48,053,323...48,095,131
JBrowse link
G MGMT O-6-methylguanine-DNA methyltransferase disease_progression IAGP DNA:hypermethylation:promoter (human) RGD PMID:15799820 RGD:2317684 NCBI chr10:129,467,241...129,770,983
Ensembl chr10:129,467,190...129,770,983
JBrowse link
G MTR 5-methyltetrahydrofolate-homocysteine methyltransferase susceptibility IAGP DNA:SNP::2756A>G(human) RGD PMID:20310006 RGD:8694083 NCBI chr 1:236,794,304...236,903,981
Ensembl chr 1:236,795,292...236,921,278
JBrowse link
G MUTYH mutY DNA glycosylase IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:25741868, PMID:26947005, PMID:28135145, PMID:28492532 NCBI chr 1:45,329,242...45,340,447
Ensembl chr 1:45,329,163...45,340,893
JBrowse link
G NF1 neurofibromin 1 IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:25741868, PMID:28492532 NCBI chr17:31,094,927...31,377,677
Ensembl chr17:31,094,927...31,382,116
JBrowse link
G NUDT15 nudix hydrolase 15 IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:8099255, PMID:12541220, PMID:28492532, PMID:28575107, PMID:29568217 NCBI chr13:48,037,726...48,052,755
Ensembl chr13:48,037,726...48,047,221
JBrowse link
G PALB2 partner and localizer of BRCA2 IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:23555315, PMID:25741868, PMID:28492532 NCBI chr16:23,603,162...23,641,337
Ensembl chr16:23,603,160...23,641,310
JBrowse link
G PTCH1 patched 1 IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:24728327, PMID:25741868, PMID:28492532 NCBI chr 9:95,442,980...95,516,971
Ensembl chr 9:95,442,980...95,517,057
JBrowse link
G RB1 RB transcriptional corepressor 1 IAGP DNA:mutations:exon, intron:multiple
ClinVar Annotator: match by term: Retinoblastoma
ClinVar
OMIM
PMID:1298292, PMID:1352883, PMID:1881452, PMID:2181449, PMID:2594029, PMID:2601691, PMID:2673542, PMID:2748600, PMID:7704558, PMID:7795591, PMID:7881418, PMID:7981694, PMID:8099255, PMID:8346255, PMID:8364580, PMID:8605116, PMID:8651278, PMID:8776589, PMID:9311732, PMID:9341870, PMID:9400934, PMID:9632788, PMID:9671401, PMID:9973307, PMID:10023315, PMID:10486322, PMID:10617920, PMID:10671068, PMID:10966849, PMID:10991691, PMID:11189328, PMID:11317357, PMID:11317369, PMID:11668642, PMID:12016586, PMID:12173465, PMID:12402348, PMID:12541220, PMID:12955724, PMID:14722923, PMID:15166261, PMID:15605413, PMID:15643604, PMID:15776430, PMID:15884040, PMID:16127685, PMID:16269091, PMID:16343894, PMID:16449662, PMID:16463005, PMID:16595082, PMID:16988938, PMID:17096365, PMID:17299438, PMID:17960112, PMID:17996702, PMID:18000883, PMID:18181215, PMID:18449911, PMID:18677112, PMID:18682685, PMID:19280657, PMID:19339519, PMID:19390654, PMID:19491728, PMID:20041224, PMID:20059380, PMID:20090211, PMID:20447117, PMID:20594292, PMID:20596833, PMID:21505449, PMID:21520333, PMID:21654082, PMID:21763628, PMID:22084214, PMID:22180099, PMID:22205104, PMID:22219649, PMID:22328814, PMID:22703879, PMID:22909775, PMID:22963398, PMID:23301675, PMID:23532519, PMID:23595191, PMID:23981928, PMID:24033266, PMID:24078560, PMID:24082139, PMID:24225018, PMID:24336570, PMID:24347427, PMID:24448499, PMID:24688104, PMID:24728327, PMID:24791139, PMID:24810223, PMID:25157968, PMID:25424699, PMID:25525159, PMID:25602518, PMID:25712084, PMID:25741868, PMID:25754945, PMID:25758528, PMID:25928201, PMID:26084579, PMID:26332594, PMID:26396485, PMID:26530098, PMID:26539030, PMID:26580448, PMID:26764160, PMID:26787237, PMID:26925970, PMID:27021801, PMID:27153395, PMID:27155049, PMID:27283993, PMID:27582626, PMID:27879208, PMID:27983729, PMID:28193182, PMID:28401291, PMID:28492532, PMID:28575107, PMID:28580595, PMID:28724667, PMID:28803391, PMID:28875981, PMID:29261756, PMID:29568217, PMID:30031154, PMID:30311386, PMID:12402348 RGD:8547986 NCBI chr13:48,303,751...48,481,890
Ensembl chr13:48,303,744...48,599,436
Ensembl chr13:48,303,744...48,599,436
JBrowse link
G SERPINF1 serpin family F member 1 treatment IDA human protein and tumor xenograft in a mouse model RGD PMID:19832843 RGD:8554870 NCBI chr17:1,762,060...1,777,565
Ensembl chr17:1,762,029...1,777,565
JBrowse link
G SNCG synuclein gamma IEP RGD PMID:18728752 RGD:6218971 NCBI chr10:86,955,759...86,963,260
Ensembl chr10:86,958,599...86,963,258
JBrowse link
G STK11 serine/threonine kinase 11 IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:25741868, PMID:28135145, PMID:28492532 NCBI chr19:1,205,778...1,228,431
Ensembl chr19:1,177,558...1,228,431
Ensembl chr19:1,177,558...1,228,431
JBrowse link
G TSC2 TSC complex subunit 2 IAGP ClinVar Annotator: match by term: Retinoblastoma ClinVar PMID:22703879, PMID:25741868, PMID:28492532 NCBI chr16:2,047,804...2,089,491
Ensembl chr16:2,047,967...2,089,491
JBrowse link
trilateral retinoblastoma term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G RB1 RB transcriptional corepressor 1 IAGP ClinVar Annotator: match by term: Retinoblastoma, trilateral ClinVar PMID:7704558, PMID:8346255, PMID:8605116, PMID:9400934, PMID:16463005, PMID:22963398, PMID:24688104, PMID:25157968, PMID:25602518, PMID:25741868, PMID:28492532 NCBI chr13:48,303,751...48,481,890
Ensembl chr13:48,303,744...48,599,436
Ensembl chr13:48,303,744...48,599,436
JBrowse link
uveal melanoma term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G BAP1 BRCA1 associated protein 1 disease_progression IEP
EXP
mRNA,protein:decreased expression: :
CTD Direct Evidence: marker/mechanism
CTD PMID:21874000, PMID:25231345, PMID:26719535, PMID:25147369 RGD:9586037 NCBI chr 3:52,401,004...52,410,030
Ensembl chr 3:52,401,008...52,410,008
JBrowse link
G BRCA2 BRCA2 DNA repair associated susceptibility IAGP DNA:mutations: : RGD PMID:22187320 RGD:9068467 NCBI chr13:32,315,508...32,400,268
Ensembl chr13:32,315,086...32,400,268
Ensembl chr13:32,315,086...32,400,268
JBrowse link
G CRP C-reactive protein disease_progression IEP RGD PMID:23057648 RGD:9491834 NCBI chr 1:159,712,289...159,714,589
Ensembl chr 1:159,712,289...159,714,589
JBrowse link
G CYSLTR2 cysteinyl leukotriene receptor 2 EXP CTD Direct Evidence: marker/mechanism CTD PMID:27089179 NCBI chr13:48,653,929...48,711,226
Ensembl chr13:48,653,711...48,711,226
JBrowse link
G EIF1AX eukaryotic translation initiation factor 1A X-linked EXP CTD Direct Evidence: marker/mechanism CTD PMID:23793026 NCBI chr  X:20,124,525...20,141,838
Ensembl chr  X:20,124,525...20,141,838
JBrowse link
G GNA11 G protein subunit alpha 11 EXP
IAGP
CTD Direct Evidence: marker/mechanism
ClinVar Annotator: match by term: Melanoma of the Uvea
CTD
ClinVar
PMID:1328859, PMID:2549426, PMID:21083380, PMID:21444680, PMID:22733540, PMID:22808163, PMID:24141786, PMID:25157968, PMID:26397223, PMID:26619011, PMID:27089179 NCBI chr19:3,094,362...3,123,999
Ensembl chr19:3,094,362...3,123,999
JBrowse link
G GNAQ G protein subunit alpha q EXP
IAGP
CTD Direct Evidence: marker/mechanism
ClinVar Annotator: match by term: Melanoma of the Uvea
CTD
ClinVar
PMID:1328859, PMID:2549426, PMID:18719078, PMID:19078957, PMID:21083380, PMID:22253748, PMID:22653968, PMID:22733540, PMID:22808163, PMID:25157968, PMID:26397223, PMID:27089179 NCBI chr 9:77,716,097...78,031,811
Ensembl chr 9:77,716,097...78,031,811
JBrowse link
G GRM1 glutamate metabotropic receptor 1 ISS OMIM:155720 | OMIM:606660 | OMIM:606661 MouseDO NCBI chr 6:146,027,634...146,437,601
Ensembl chr 6:146,027,646...146,437,601
JBrowse link
G HLA-B major histocompatibility complex, class I, B severity IEP protein:increased expression:tumor of uvea (human) RGD PMID:9286277 RGD:7364941 NCBI chr 6:31,353,875...31,357,179
Ensembl chr 6:31,269,491...31,357,188
JBrowse link
G IGF1 insulin like growth factor 1 disease_progression IEP RGD PMID:23197685 RGD:8548834 NCBI chr12:102,395,860...102,481,839
Ensembl chr12:102,395,874...102,481,744
JBrowse link
G JMJD6 jumonji domain containing 6, arginine demethylase and lysine hydroxylase EXP CTD Direct Evidence: marker/mechanism CTD PMID:30619488 NCBI chr17:76,712,830...76,726,783
Ensembl chr17:76,712,832...76,726,799
JBrowse link
G KDM5B lysine demethylase 5B severity IEP protein:increased expression:uvea (human) RGD PMID:22669717 RGD:9587775 NCBI chr 1:202,724,495...202,809,470
Ensembl chr 1:202,724,495...202,808,487
Ensembl chr 1:202,724,495...202,808,487
JBrowse link
G KDR kinase insert domain receptor disease_progression IEP RGD PMID:21984395 RGD:8549718 NCBI chr 4:55,078,481...55,125,595
Ensembl chr 4:55,078,481...55,125,595
JBrowse link
G MCAM melanoma cell adhesion molecule disease_progression IEP RGD PMID:19958117 RGD:7364775 NCBI chr11:119,305,759...119,317,130
Ensembl chr11:119,308,529...119,321,521
JBrowse link
G PLCB4 phospholipase C beta 4 EXP
IAGP
CTD Direct Evidence: marker/mechanism
ClinVar Annotator: match by term: Uveal melanoma
CTD
ClinVar
PMID:27089179, PMID:31186267 NCBI chr20:9,068,678...9,480,808
Ensembl chr20:9,068,763...9,481,242
JBrowse link
G PRAME PRAME nuclear receptor transcriptional regulator severity IEP mRNA:increased expression:uvea (human) RGD PMID:27486988 RGD:11535039 NCBI chr22:22,547,701...22,559,294
Ensembl chr22:22,547,701...22,559,361
JBrowse link
G SERPINE1 serpin family E member 1 treatment IMP human gene in mouse model RGD PMID:9326241 RGD:8547806 NCBI chr 7:101,127,104...101,139,247
Ensembl chr 7:101,127,104...101,139,247
Ensembl chr 7:101,127,104...101,139,247
JBrowse link
G SERPINF1 serpin family F member 1 severity ISO RGD PMID:23793989 RGD:8554893 NCBI chr17:1,762,060...1,777,565
Ensembl chr17:1,762,029...1,777,565
JBrowse link
G SF3B1 splicing factor 3b subunit 1 EXP CTD Direct Evidence: marker/mechanism CTD PMID:23313955, PMID:23793026 NCBI chr 2:197,389,784...197,435,093
Ensembl chr 2:197,388,515...197,435,091
Ensembl chr 2:197,388,515...197,435,091
JBrowse link
G TMEM127 transmembrane protein 127 IAGP ClinVar Annotator: match by term: Uveal melanoma ClinVar PMID:25741868, PMID:28492532 NCBI chr 2:96,248,514...96,265,997
Ensembl chr 2:96,248,516...96,265,994
Ensembl chr 2:96,248,516...96,265,994
JBrowse link
G VEGFA vascular endothelial growth factor A IEP protein:increased expression:iris, ciliary body, vitreous body; RGD PMID:11914216 RGD:7483591 NCBI chr 6:43,770,209...43,786,487
Ensembl chr 6:43,770,184...43,786,487
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18864
    Pathological Conditions, Signs and Symptoms 9687
      Signs and Symptoms 5971
        Neurologic Manifestations 4794
          Sensation Disorders 1232
            Somatosensory Disorders 451
              Benign Cerebellar Ataxia with Thermoanalgesia 0
              Distal Arthrogryposis, with Impaired Proprioception and Touch 1
              Hyperalgesia 194
              Hyperesthesia 1
              Hypesthesia + 4
              Hypoalgesia 2
              Paresthesia 4
              sensory system cancer + 247
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.