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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:PTEN hamartoma tumor syndrome
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Accession:DOID:0080191 term browser browse the term
Definition:A syndrome characterized as a spectrum of disorders (Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, PTEN-related Proteus syndrome, and Proteus-like syndrome) caused by germline mutations of the PTEN gene. (DO)
Synonyms:exact_synonym: CS;   Multiple Hamartoma Syndrome;   PTEN hamartoma tumor syndrome with granular cell tumor;   multiple hamartoma syndromes
 narrow_synonym: Colorectal hamartomatous polyposis and ganglioneuromatosis;   MHAM DYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM;   PROTEUS-like syndrome;   cerebellar granule cell hypertrophy and megalencephaly;   cerebelloparenchymal disorder VI
 primary_id: MESH:D006223
 alt_id: MESH:C566636;   OMIA:001515
 xref: GARD:12800
For additional species annotation, visit the Alliance of Genome Resources.


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PTEN hamartoma tumor syndrome term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G ACTA2 actin alpha 2, smooth muscle ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:18456716, PMID:21926107, PMID:22382802, PMID:23132533, PMID:23335809, PMID:28492532 NCBI chr10:85,660,983...85,678,729
Ensembl chr10:89,164,344...89,182,080
JBrowse link
G ADIRF adipogenesis regulatory factor ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:28492532 NCBI chr10:83,395,796...83,428,549
Ensembl chr10:86,952,714...86,955,219
JBrowse link
G AGAP11 ArfGAP with GTPase domain, ankyrin repeat and PH domain 11 ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:28492532 NCBI chr10:83,436,331...83,458,130 JBrowse link
G ANKRD22 ankyrin repeat domain 22 ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:18456716, PMID:21926107, PMID:22382802, PMID:23132533, PMID:23335809, PMID:28492532 NCBI chr10:85,546,939...85,577,698
Ensembl chr10:89,048,724...89,081,637
JBrowse link
G ATAD1 ATPase family AAA domain containing 1 ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:16287957, PMID:16685657, PMID:18456716, PMID:18510548, PMID:23335809, PMID:28492532 NCBI chr10:84,473,087...84,544,902
Ensembl chr10:87,981,974...88,048,228
JBrowse link
G BMPR1A bone morphogenetic protein receptor type 1A ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:28492532 NCBI chr10:83,185,040...83,353,239
Ensembl chr10:86,837,469...86,912,912
JBrowse link
G FAM25A family with sequence similarity 25 member A ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:28492532 NCBI chr10:83,468,123...83,472,559 JBrowse link
G FGFR2 fibroblast growth factor receptor 2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:9002682 NCBI chr10:118,055,854...118,175,440
Ensembl chr10:121,469,735...121,588,815
JBrowse link
G GLUD1 glutamate dehydrogenase 1 ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:28492532 NCBI chr10:83,498,338...83,540,730 JBrowse link
G KLLN killin, p53 regulated DNA replication inhibitor ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:2338203, PMID:11906179, PMID:12844284, PMID:16052674, PMID:16287957, PMID:16685657, PMID:16773562, PMID:17427195, PMID:18456716, PMID:18510548, PMID:20862607, PMID:21194675, PMID:21417916, PMID:21532617, PMID:21926107, PMID:21956414, PMID:22382802, PMID:22595938, PMID:23132533, PMID:23335809, PMID:24033266, PMID:25669429, PMID:25741868, PMID:26229595, PMID:26467025, PMID:27535533, PMID:27878467, PMID:27884173, PMID:28492532, PMID:28526761 NCBI chr10:84,581,971...84,587,420 JBrowse link
G LIPF lipase F, gastric type ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:16287957, PMID:16685657, PMID:18456716, PMID:18510548, PMID:21926107, PMID:22382802, PMID:23132533, PMID:23335809, PMID:28492532 NCBI chr10:85,389,165...85,403,492
Ensembl chr10:88,892,525...88,906,898
JBrowse link
G LIPJ lipase family member J ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:16287957, PMID:16685657, PMID:18456716, PMID:18510548, PMID:21926107, PMID:22382802, PMID:23132533, PMID:23335809, PMID:28492532 NCBI chr10:85,307,536...85,330,911
Ensembl chr10:88,816,492...88,832,860
JBrowse link
G LIPK lipase family member K ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:16287957, PMID:16685657, PMID:18456716, PMID:18510548, PMID:21926107, PMID:22382802, PMID:23132533, PMID:23335809, PMID:28492532 NCBI chr10:85,430,807...85,478,506
Ensembl chr10:88,952,502...88,981,951
JBrowse link
G LIPM lipase family member M ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:18456716, PMID:21926107, PMID:22382802, PMID:23132533, PMID:23335809, PMID:28492532 NCBI chr10:85,528,337...85,547,789
Ensembl chr10:89,031,764...89,049,607
JBrowse link
G LIPN lipase family member N ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:16287957, PMID:16685657, PMID:18456716, PMID:18510548, PMID:21926107, PMID:22382802, PMID:23132533, PMID:23335809, PMID:28492532 NCBI chr10:85,485,727...85,505,268
Ensembl chr10:88,990,571...89,007,327
JBrowse link
G MINPP1 multiple inositol-polyphosphate phosphatase 1 ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:16287957, PMID:16685657, PMID:18456716, PMID:18510548, PMID:23335809, PMID:28492532 NCBI chr10:84,230,676...84,280,042
Ensembl chr10:87,737,649...87,787,130
JBrowse link
G MMRN2 multimerin 2 ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:28492532 NCBI chr10:83,363,696...83,396,966
Ensembl chr10:86,920,521...86,942,777
JBrowse link
G PAPSS2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:16287957, PMID:16685657, PMID:18456716, PMID:18510548, PMID:23335809, PMID:28492532 NCBI chr10:84,383,936...84,471,745
Ensembl chr10:87,890,631...87,977,839
JBrowse link
G PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha ISO ClinVar Annotator: match by term: Multiple hamartoma syndrome ClinVar PMID:15930273, PMID:17376864, PMID:19366826, PMID:21824802, PMID:22120714, PMID:22729224, PMID:22949682, PMID:24033266, PMID:25157968, PMID:25741868, PMID:26619011, PMID:27631024, PMID:28492532, PMID:28941273, PMID:30311386, PMID:31568861 NCBI chr 3:176,182,765...176,272,024
Ensembl chr 3:184,355,785...184,441,977
JBrowse link
G PTEN phosphatase and tensin homolog susceptibility ISO DNA:missense mutation, nonsense mutations:cds:p.G129E, p.E157X, p.R233X (human)
ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome
DNA:deletion:exon:c.950_953delTACT (human)
mRNA:spice variants:lymphocyte (human)
DNA:deletions:multiple (human)
CTD Direct Evidence: marker/mechanism
RGD
ClinVar
CTD
PMID:1097835, PMID:2338203, PMID:7728760, PMID:8071972, PMID:8673088, PMID:8980400, PMID:9140396, PMID:9241266, PMID:9256433, PMID:9259288, PMID:9286463, PMID:9288766, PMID:9326929, PMID:9371490, PMID:9399897, PMID:9425889, PMID:9467011, PMID:9598803, PMID:9600246, PMID:9619835, PMID:9685848, PMID:9697695, PMID:9735393, PMID:9740666, PMID:9788441, PMID:9794233, PMID:9797362, PMID:9832031, PMID:9832032, PMID:9856571, PMID:9915974, PMID:10051603, PMID:10076877, PMID:10232405, PMID:10234502, PMID:10353779, PMID:10400993, PMID:10468583, PMID:10555148, PMID:10606430, PMID:10698513, PMID:10749983, PMID:10772829, PMID:10777358, PMID:10807691, PMID:10848731, PMID:10866302, PMID:10866658, PMID:10920277, PMID:10923032, PMID:10959096, PMID:10978354, PMID:11035045, PMID:11052475, PMID:11071384, PMID:11108659, PMID:11156408, PMID:11238682, PMID:11274365, PMID:11332402, PMID:11355302, PMID:11476841, PMID:11494117, PMID:11496368, PMID:11504908, PMID:11685670, PMID:11748304, PMID:11875759, PMID:11886535, PMID:11906179, PMID:11918710, PMID:11939587, PMID:11948419, PMID:12085208, PMID:12208743, PMID:12297295, PMID:12372056, PMID:12471211, PMID:12614768, PMID:12788938, PMID:12844284, PMID:12938083, PMID:14518070, PMID:14566704, PMID:14574156, PMID:14623110, PMID:14675182, PMID:15016963, PMID:15120218, PMID:15211648, PMID:15254419, PMID:15372512, PMID:15647370, PMID:15659546, PMID:15769473, PMID:15805158, PMID:15896465, PMID:15987703, PMID:16007494, PMID:16014636, PMID:16021145, PMID:16052674, PMID:16287957, PMID:16506206, PMID:16598737, PMID:16619501, PMID:16685657, PMID:16704655, PMID:16752378, PMID:16773562, PMID:16829519, PMID:16894538, PMID:16952599, PMID:17043057, PMID:17218260, PMID:17218261, PMID:17286265, PMID:17324556, PMID:17341483, PMID:17392703, PMID:17427195, PMID:17444818, PMID:17526800, PMID:17526801, PMID:17636424, PMID:17847000, PMID:17873119, PMID:17873882, PMID:17898811, PMID:17928923, PMID:17941496, PMID:17942903, PMID:17954274, PMID:18080326, PMID:18456716, PMID:18510548, PMID:18558293, PMID:18716620, PMID:18725974, PMID:18759867, PMID:18767981, PMID:18794879, PMID:19265751, PMID:19321504, PMID:19329485, PMID:19340001, PMID:19351834, PMID:19366826, PMID:19457929, PMID:19458356, PMID:19668082, PMID:19719509, PMID:19763152, PMID:19829307, PMID:19903786, PMID:19956187, PMID:19968660, PMID:20018398, PMID:20085938, PMID:20186503, PMID:20194734, PMID:20223021, PMID:20300775, PMID:20307669, PMID:20395440, PMID:20453058, PMID:20533527, PMID:20538496, PMID:20600018, PMID:20619739, PMID:20712882, PMID:20718038, PMID:20862607, PMID:20881644, PMID:20926450, PMID:20962022, PMID:21103832, PMID:21194575, PMID:21194675, PMID:21291452, PMID:21343951, PMID:21417916, PMID:21532617, PMID:21659347, PMID:21822720, PMID:21824802, PMID:21828076, PMID:21869887, PMID:21926107, PMID:21956414, PMID:22076652, PMID:22162582, PMID:22162589, PMID:22252256, PMID:22261759, PMID:22266152, PMID:22281088, PMID:22320991, PMID:22327138, PMID:22381246, PMID:22382802, PMID:22406018, PMID:22469695, PMID:22479427, PMID:22491738, PMID:22503188, PMID:22505997, PMID:22520842, PMID:22529920, PMID:22558107, PMID:22595938, PMID:22628360, PMID:22703879, PMID:22713753, PMID:22962422, PMID:23066114, PMID:23117110, PMID:23124040, PMID:23132533, PMID:23160955, PMID:23161105, PMID:23315997, PMID:23335809, PMID:23349303, PMID:23382303, PMID:23399955, PMID:23419777, PMID:23423780, PMID:23442912, PMID:23470840, PMID:23475934, PMID:23555315, PMID:23633456, PMID:23695273, PMID:23757202, PMID:23764071, PMID:23886400, PMID:23934111, PMID:23934601, PMID:24004025, PMID:24033266, PMID:24052722, PMID:24055113, PMID:24102544, PMID:24136893, PMID:24292679, PMID:24345843, PMID:24375884, PMID:24379037, PMID:24468202, PMID:24483290, PMID:24498881, PMID:24500884, PMID:24641667, PMID:24647592, PMID:24656772, PMID:24721394, PMID:24728327, PMID:24744697, PMID:24763289, PMID:24778394, PMID:24905788, PMID:25022750, PMID:25132236, PMID:25157968, PMID:25186627, PMID:25246819, PMID:25288137, PMID:25326635, PMID:25336918, PMID:25363760, PMID:25418537, PMID:25429968, PMID:25448478, PMID:25448482, PMID:25525159, PMID:25527629, PMID:25549896, PMID:25647146, PMID:25669429, PMID:25722288, PMID:25741868, PMID:25756585, PMID:25875300, PMID:25910213, PMID:25937288, PMID:25980754, PMID:26076150, PMID:26124082, PMID:26157835, PMID:26185318, PMID:26216063, PMID:26229595, PMID:26246517, PMID:26279303, PMID:26350204, PMID:26362251, PMID:26376867, PMID:26443266, PMID:26467025, PMID:26468640, PMID:26504226, PMID:26517354, PMID:26534844, PMID:26579216, PMID:26580448, PMID:26619011, PMID:26633542, PMID:26681312, PMID:26773036, PMID:26787237, PMID:26795104, PMID:26798346, PMID:26800850, PMID:26845104, PMID:26898890, PMID:27087592, PMID:27157322, PMID:27426521, PMID:27428751, PMID:27477328, PMID:27514801, PMID:27531073, PMID:27535533, PMID:27720647, PMID:27824329, PMID:27878467, PMID:27884173, PMID:27978560, PMID:28086757, PMID:28135145, PMID:28191890, PMID:28195393, PMID:28250423, PMID:28263302, PMID:28263967, PMID:28286253, PMID:28418444, PMID:28475857, PMID:28492532, PMID:28497778, PMID:28513612, PMID:28523199, PMID:28526761, PMID:28600779, PMID:28655553, PMID:28677221, PMID:28724667, PMID:28774669, PMID:29043291, PMID:29048666, PMID:29117568, PMID:29273943, PMID:29296277, PMID:29359449, PMID:29373119, PMID:29510612, PMID:29608813, PMID:29663862, PMID:29706350, PMID:29706633, PMID:29706646, PMID:29752200, PMID:29785012, PMID:29874181, PMID:29970488, PMID:30043523, PMID:30287823, PMID:30311380, PMID:30311381, PMID:30311386, PMID:30327747, PMID:30482242, PMID:30793491, PMID:30809968, PMID:30993208, PMID:31006514, PMID:32238909, PMID:32566746 RGD:12802356, RGD:12802361, RGD:12859035, RGD:12859041, RGD:1302552 NCBI chr10:84,587,841...84,689,043
Ensembl chr10:88,093,539...88,194,605
JBrowse link
G RNLS renalase, FAD dependent amine oxidase ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:16287957, PMID:16685657, PMID:18456716, PMID:18510548, PMID:21926107, PMID:22382802, PMID:23132533, PMID:23335809, PMID:28492532 NCBI chr10:84,996,999...85,304,240
Ensembl chr10:88,503,683...88,808,990
JBrowse link
G SDHD succinate dehydrogenase complex subunit D ISO ClinVar Annotator: match by term: Multiple hamartoma syndrome ClinVar PMID:18678321, PMID:21565294, PMID:21979946, PMID:28492532, PMID:29386252 NCBI chr11:106,973,256...106,982,237
Ensembl chr11:110,817,016...110,896,829
JBrowse link
G SHLD2 shieldin complex subunit 2 ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:28492532 NCBI chr10:83,639,020...83,643,420 JBrowse link
G SNCG synuclein gamma ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:28492532 NCBI chr10:83,383,566...83,391,064 JBrowse link
G STAMBPL1 STAM binding protein like 1 ISO ClinVar Annotator: match by term: PTEN hamartoma tumor syndrome ClinVar PMID:18456716, PMID:21926107, PMID:22382802, PMID:23132533, PMID:23335809, PMID:28492532 NCBI chr10:85,605,651...85,649,268
Ensembl chr10:89,109,356...89,152,628
JBrowse link
Bannayan-Riley-Ruvalcaba syndrome term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha ISO ClinVar Annotator: match by term: RUVALCABA-MYHRE-SMITH SYNDROME
ClinVar Annotator: match by term: MACROCEPHALY, PSEUDOPAPILLEDEMA, AND MULTIPLE HEMANGIOMATA
ClinVar PMID:15930273, PMID:17376864, PMID:19366826, PMID:21824802, PMID:22120714, PMID:22729224, PMID:22949682, PMID:24033266, PMID:25157968, PMID:25741868, PMID:26619011, PMID:27631024, PMID:28492532, PMID:28941273, PMID:30311386, PMID:31568861 NCBI chr 3:176,182,765...176,272,024
Ensembl chr 3:184,355,785...184,441,977
JBrowse link
G PTEN phosphatase and tensin homolog ISO ClinVar Annotator: match by term: Bannayan-Riley-Ruvalcaba syndrome
ClinVar Annotator: match by term: RUVALCABA-MYHRE-SMITH SYNDROME
ClinVar Annotator: match by term: MACROCEPHALY, PSEUDOPAPILLEDEMA, AND MULTIPLE HEMANGIOMATA
ClinVar PMID:9140396, PMID:9241266, PMID:9259288, PMID:9399897, PMID:9467011, PMID:9598803, PMID:10232405, PMID:10353779, PMID:10400993, PMID:10468583, PMID:10555148, PMID:10749983, PMID:10848731, PMID:10920277, PMID:10923032, PMID:11238682, PMID:11504908, PMID:11685670, PMID:12844284, PMID:14518070, PMID:15016963, PMID:15211648, PMID:15254419, PMID:15647370, PMID:15805158, PMID:16952599, PMID:17286265, PMID:17392703, PMID:17427195, PMID:17526800, PMID:17873882, PMID:18558293, PMID:18725974, PMID:19265751, PMID:19340001, PMID:19351834, PMID:19366826, PMID:19458356, PMID:19668082, PMID:19829307, PMID:19903786, PMID:20018398, PMID:20085938, PMID:20453058, PMID:20619739, PMID:20881644, PMID:21194675, PMID:21956414, PMID:22162582, PMID:22162589, PMID:22252256, PMID:22381246, PMID:22479427, PMID:22491738, PMID:23335809, PMID:23349303, PMID:23442912, PMID:23470840, PMID:23475934, PMID:23695273, PMID:24033266, PMID:24052722, PMID:24136893, PMID:24778394, PMID:25022750, PMID:25132236, PMID:25157968, PMID:25288137, PMID:25326635, PMID:25669429, PMID:25741868, PMID:25756585, PMID:26773036, PMID:27426521, PMID:27477328, PMID:28286253, PMID:28492532, PMID:28526761, PMID:30287823, PMID:32238909 NCBI chr10:84,587,841...84,689,043
Ensembl chr10:88,093,539...88,194,605
JBrowse link
G SDHD succinate dehydrogenase complex subunit D ISO ClinVar Annotator: match by term: MACROCEPHALY, PSEUDOPAPILLEDEMA, AND MULTIPLE HEMANGIOMATA ClinVar PMID:18678321, PMID:21565294, PMID:21979946, PMID:28492532, PMID:29386252 NCBI chr11:106,973,256...106,982,237
Ensembl chr11:110,817,016...110,896,829
JBrowse link
Cowden syndrome term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G EGFR epidermal growth factor receptor ISO ClinVar Annotator: match by term: Cowden syndrome 1 ClinVar NCBI chr 7:55,614,042...55,807,285
Ensembl chr 7:56,046,296...56,111,615
JBrowse link
G KLLN killin, p53 regulated DNA replication inhibitor ISO ClinVar Annotator: match by term: Cowden syndrome 1 ClinVar PMID:2338203, PMID:12844284, PMID:16773562, PMID:17427195, PMID:21194675, PMID:21417916, PMID:21532617, PMID:24033266, PMID:25669429, PMID:25741868, PMID:26467025, PMID:27535533, PMID:27878467, PMID:27884173, PMID:28492532 NCBI chr10:84,581,971...84,587,420 JBrowse link
G PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha ISO ClinVar Annotator: match by term: Cowden syndrome
ClinVar Annotator: match by term: Cowden disease
ClinVar Annotator: match by term: Cowden syndrome 1
ClinVar Annotator: match by term: Lhermitte-Duclos Disease
ClinVar PMID:15016963, PMID:15254419, PMID:15520168, PMID:15647370, PMID:15805248, PMID:15930273, PMID:16906227, PMID:16930767, PMID:17376864, PMID:18074223, PMID:18676830, PMID:18725974, PMID:18829572, PMID:19029981, PMID:19366826, PMID:19513541, PMID:19903786, PMID:20453058, PMID:20619739, PMID:21430269, PMID:21824802, PMID:22120714, PMID:22162582, PMID:22162589, PMID:22271473, PMID:22729222, PMID:22729224, PMID:22949682, PMID:24033266, PMID:25157968, PMID:25741868, PMID:26619011, PMID:27631024, PMID:28151489, PMID:28492532, PMID:28941273, PMID:29446767, PMID:30311386, PMID:31568861 NCBI chr 3:176,182,765...176,272,024
Ensembl chr 3:184,355,785...184,441,977
JBrowse link
G PTEN phosphatase and tensin homolog ISO OMIM NCBI chr10:84,587,841...84,689,043
Ensembl chr10:88,093,539...88,194,605
JBrowse link
G RINT1 RAD50 interactor 1 ISO ClinVar Annotator: match by term: Cowden syndrome ClinVar PMID:28492532 NCBI chr 7:97,522,208...97,567,897
Ensembl chr 7:110,252,776...110,287,702
JBrowse link
G SDHB succinate dehydrogenase complex iron sulfur subunit B ISO ClinVar Annotator: match by term: Cowden syndrome
ClinVar Annotator: match by term: Cowden disease
ClinVar PMID:11404820, PMID:14985401, PMID:16314641, PMID:16317055, PMID:16322339, PMID:16912137, PMID:17102082, PMID:17102083, PMID:17298551, PMID:17376234, PMID:17639058, PMID:17987308, PMID:18551016, PMID:18678321, PMID:18753105, PMID:19351833, PMID:19368708, PMID:19399650, PMID:19454582, PMID:19802898, PMID:21979946, PMID:22517554, PMID:22703879, PMID:22995991, PMID:23072324, PMID:23660872, PMID:23666964, PMID:23735539, PMID:24033266, PMID:24659481, PMID:24728327, PMID:25047027, PMID:25333069, PMID:25694510, PMID:25741868, PMID:26092435, PMID:26269449, PMID:26729832, PMID:26960314, PMID:27604842, PMID:28229225, PMID:28492532 NCBI chr 1:15,962,383...15,998,056
Ensembl chr 1:17,018,542...17,054,509
JBrowse link
G SDHD succinate dehydrogenase complex subunit D ISO ClinVar Annotator: match by term: Cowden disease ClinVar PMID:18678321, PMID:21565294, PMID:21979946, PMID:28492532, PMID:29386252 NCBI chr11:106,973,256...106,982,237
Ensembl chr11:110,817,016...110,896,829
JBrowse link
Cowden Syndrome 4 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G KLLN killin, p53 regulated DNA replication inhibitor ISO OMIM NCBI chr10:84,581,971...84,587,420 JBrowse link
Cowden Syndrome 5 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha ISO OMIM NCBI chr 3:176,182,765...176,272,024
Ensembl chr 3:184,355,785...184,441,977
JBrowse link
Cowden Syndrome 6 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G AKT1 AKT serine/threonine kinase 1 ISO OMIM NCBI chr14:85,417,229...85,444,722
Ensembl chr14:105,208,128...105,236,756
JBrowse link
Cowden Syndrome 7 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G SEC23B SEC23 homolog B, COPII coat complex component ISO OMIM NCBI chr20:18,469,182...18,523,114
Ensembl chr20:18,440,121...18,493,512
JBrowse link
Cowden-Like Syndrome term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha ISO ClinVar Annotator: match by term: Cowden syndrome 2 ClinVar PMID:15930273, PMID:17376864, PMID:19366826, PMID:21824802, PMID:22120714, PMID:22729224, PMID:22949682, PMID:24033266, PMID:25157968, PMID:25741868, PMID:26619011, PMID:27631024, PMID:28492532, PMID:28941273, PMID:30311386, PMID:31568861 NCBI chr 3:176,182,765...176,272,024
Ensembl chr 3:184,355,785...184,441,977
JBrowse link
G PTEN phosphatase and tensin homolog ISO ClinVar Annotator: match by term: Cowden syndrome 2 ClinVar PMID:9140396, PMID:9241266, PMID:9259288, PMID:9399897, PMID:9467011, PMID:9598803, PMID:10232405, PMID:10353779, PMID:10400993, PMID:10468583, PMID:10555148, PMID:10749983, PMID:10848731, PMID:10920277, PMID:10923032, PMID:11238682, PMID:11504908, PMID:11685670, PMID:12844284, PMID:14518070, PMID:15016963, PMID:15211648, PMID:15254419, PMID:15647370, PMID:15805158, PMID:16952599, PMID:17286265, PMID:17392703, PMID:17427195, PMID:17526800, PMID:17873882, PMID:18558293, PMID:18725974, PMID:19265751, PMID:19340001, PMID:19351834, PMID:19366826, PMID:19458356, PMID:19668082, PMID:19829307, PMID:19903786, PMID:20018398, PMID:20085938, PMID:20453058, PMID:20619739, PMID:20881644, PMID:21194675, PMID:21956414, PMID:22162582, PMID:22162589, PMID:22252256, PMID:22381246, PMID:22479427, PMID:22491738, PMID:23335809, PMID:23349303, PMID:23442912, PMID:23470840, PMID:23475934, PMID:23695273, PMID:24033266, PMID:24052722, PMID:24136893, PMID:24778394, PMID:25022750, PMID:25132236, PMID:25157968, PMID:25288137, PMID:25326635, PMID:25669429, PMID:25741868, PMID:25756585, PMID:26773036, PMID:27426521, PMID:27477328, PMID:28286253, PMID:28492532, PMID:28526761, PMID:30287823, PMID:32238909 NCBI chr10:84,587,841...84,689,043
Ensembl chr10:88,093,539...88,194,605
JBrowse link
G SDHD succinate dehydrogenase complex subunit D ISO ClinVar Annotator: match by term: Cowden syndrome 2 ClinVar PMID:18678321, PMID:21565294, PMID:21979946, PMID:28492532, PMID:29386252 NCBI chr11:106,973,256...106,982,237
Ensembl chr11:110,817,016...110,896,829
JBrowse link
Macrocephaly Mesodermal Hamartoma Spectrum term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G AKT1 AKT serine/threonine kinase 1 ISO ClinVar Annotator: match by term: Elattoproteus syndrome ClinVar PMID:17611497, PMID:18256540, PMID:18392055, PMID:18504432, PMID:18611285, PMID:19418217, PMID:19487299, PMID:19853286, PMID:20233444, PMID:20453058, PMID:21464312, PMID:21512767, PMID:21793738, PMID:22538770, PMID:22610119, PMID:22722201, PMID:22722839, PMID:22980975, PMID:23237847, PMID:23348505, PMID:23700467, PMID:23728071, PMID:23934607, PMID:24190505, PMID:24657128, PMID:25157968, PMID:26619011, PMID:28492532 NCBI chr14:85,417,229...85,444,722
Ensembl chr14:105,208,128...105,236,756
JBrowse link
Proteus syndrome term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G AKT1 AKT serine/threonine kinase 1 ISO OMIM NCBI chr14:85,417,229...85,444,722
Ensembl chr14:105,208,128...105,236,756
JBrowse link
G PTEN phosphatase and tensin homolog ISO CTD Direct Evidence: marker/mechanism
ClinVar Annotator: match by term: Proteus-like syndrome
CTD
ClinVar
PMID:9399897, PMID:9467011, PMID:10232405, PMID:10353779, PMID:10400993, PMID:10468583, PMID:10749983, PMID:10848731, PMID:11238682, PMID:11685670, PMID:11748304, PMID:12471211, PMID:12844284, PMID:14518070, PMID:15805158, PMID:17286265, PMID:17392703, PMID:17427195, PMID:19265751, PMID:19668082, PMID:21194675, PMID:21956414, PMID:22252256, PMID:22381246, PMID:23442912, PMID:23470840, PMID:23475934, PMID:23695273, PMID:24033266, PMID:24052722, PMID:24136893, PMID:24778394, PMID:25022750, PMID:25132236, PMID:25157968, PMID:25326635, PMID:25669429, PMID:25741868, PMID:25756585, PMID:27477328, PMID:27535533, PMID:28492532, PMID:28526761, PMID:30287823, PMID:32238909 NCBI chr10:84,587,841...84,689,043
Ensembl chr10:88,093,539...88,194,605
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12749
    disease of cellular proliferation 5477
      Multiple Primary Neoplasms 143
        PTEN hamartoma tumor syndrome 30
          Bannayan-Riley-Ruvalcaba syndrome 3
          Cerebellar Granule Cell Hypertrophy and Megalencephaly 0
          Cerebelloparenchymal Disorder VI 0
          Cowden syndrome + 9
          Cowden-Like Syndrome 3
          Graham Boyle Troxell Syndrome 0
          Heart Defect, Tongue Hamartoma and Polysyndactyly 0
          Multiple Basal Cell Carcinoma 0
          Proteus syndrome + 2
          Sacral Hemangiomas Multiple Congenital Abnormalities 0
Path 2
Term Annotations click to browse term
  disease 12749
    Developmental Diseases 9004
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7853
        genetic disease 7377
          Hereditary Neoplastic Syndromes 780
            PTEN hamartoma tumor syndrome 30
              Bannayan-Riley-Ruvalcaba syndrome 3
              Cerebellar Granule Cell Hypertrophy and Megalencephaly 0
              Cerebelloparenchymal Disorder VI 0
              Cowden syndrome + 9
              Cowden-Like Syndrome 3
              Graham Boyle Troxell Syndrome 0
              Heart Defect, Tongue Hamartoma and Polysyndactyly 0
              Multiple Basal Cell Carcinoma 0
              Proteus syndrome + 2
              Sacral Hemangiomas Multiple Congenital Abnormalities 0
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.