Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

ONTOLOGY REPORT - ANNOTATIONS


Term:myopia
go back to main search page
Accession:DOID:11830 term browser browse the term
Definition:A refractive error in which rays of light entering the EYE parallel to the optic axis are brought to a focus in front of the RETINA when accommodation (ACCOMMODATION, OCULAR) is relaxed. This results from an overly curved CORNEA or from the eyeball being too long from front to back. It is also called nearsightedness.
Synonyms:exact_synonym: myopias;   near vision;   near-sightedness;   nearsightedness;   short-sightedness
 primary_id: MESH:D009216
 xref: ICD10CM:H52.1;   ICD9CM:367.1;   NCI:C102533;   OMIM:PS160700
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
myopia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Adora2a adenosine A2a receptor JBrowse link 20 14,265,251 14,282,873 RGD:13592920
G Bmp2 bone morphogenetic protein 2 JBrowse link 3 126,335,963 126,346,771 RGD:11554173
G Cacna1f calcium voltage-gated channel subunit alpha1 F JBrowse link X 15,712,709 15,741,135 RGD:8554872
G Chd7 chromodomain helicase DNA binding protein 7 JBrowse link 5 21,769,087 21,952,036 RGD:8554872
G Col1a1 collagen type I alpha 1 chain JBrowse link 10 82,745,801 82,762,790 RGD:8552656
G Col2a1 collagen type II alpha 1 chain JBrowse link 7 139,454,945 139,484,403 RGD:8657390
RGD:8554872
RGD:12436723
RGD:11554173
G Col9a1 collagen type IX alpha 1 chain JBrowse link 9 30,419,001 30,502,307 RGD:11554173
G Fbn1 fibrillin 1 JBrowse link 3 117,569,708 117,766,160 RGD:8554872
G Gjd2 gap junction protein, delta 2 JBrowse link 3 105,467,480 105,470,475 RGD:11554173
G Gria4 glutamate ionotropic receptor AMPA type subunit 4 JBrowse link 8 1,548,145 2,045,874 RGD:11554173
G Hgf hepatocyte growth factor JBrowse link 4 15,435,460 15,505,377 RGD:1642706
RGD:8548600
RGD:8548542
G Igf1 insulin-like growth factor 1 JBrowse link 7 28,412,123 28,491,815 RGD:8548827
RGD:8548838
RGD:8548829
RGD:8548828
G Irx5 iroquois homeobox 5 JBrowse link 19 16,415,813 16,421,088 RGD:11554173
G Kcnq5 potassium voltage-gated channel subfamily Q member 5 JBrowse link 9 27,565,869 28,141,114 RGD:11554173
G Lama2 laminin subunit alpha 2 JBrowse link 1 18,491,264 19,143,486 RGD:11554173
RGD:13605610
G Lrpap1 LDL receptor related protein associated protein 1 JBrowse link 14 80,911,281 80,923,290 RGD:13592920
G Mmp2 matrix metallopeptidase 2 JBrowse link 19 15,542,771 15,570,589 RGD:8549731
G Parl presenilin associated, rhomboid-like JBrowse link 11 84,517,368 84,544,463 RGD:12902630
G Primpol primase and DNA directed polymerase JBrowse link 16 48,863,385 48,900,409 RGD:13592920
G Prss56 serine protease 56 JBrowse link 9 94,278,981 94,284,111 RGD:11554173
G Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 JBrowse link 8 97,277,250 97,405,095 RGD:11554173
G Rdh5 retinol dehydrogenase 5 JBrowse link 7 3,335,681 3,342,573 RGD:11554173
G Six6 SIX homeobox 6 JBrowse link 6 95,816,749 95,821,729 RGD:11554173
G Slc25a4 solute carrier family 25 member 4 JBrowse link 16 49,266,903 49,270,698 RGD:8554872
G Slc39a13 solute carrier family 39 member 13 JBrowse link 3 79,884,524 79,892,664 RGD:8554872
G Slc39a5 solute carrier family 39 member 5 JBrowse link 7 2,813,875 2,819,917 RGD:13592920
G Tnc tenascin C JBrowse link 5 79,789,686 79,874,555 RGD:8554872
G Tyr tyrosinase JBrowse link 1 151,012,598 151,106,802 RGD:8554872
G Vdr vitamin D receptor JBrowse link 7 139,344,452 139,394,138 RGD:8157620
G Vps13b vacuolar protein sorting 13 homolog B JBrowse link 7 74,118,834 74,722,341 RGD:8554872
G Zfp469 zinc finger protein 469 JBrowse link 19 54,843,864 55,083,935 RGD:8554872
G Zfp644 zinc finger protein 644 JBrowse link 14 4,125,368 4,200,332 RGD:13592920
Cochlear Deafness with Myopia and Intellectual Impairment term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Slitrk6 SLIT and NTRK-like family, member 6 JBrowse link 15 95,507,632 95,514,259 RGD:8554872
Cohen syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mir875 microRNA 875 JBrowse link 7 74,423,233 74,423,305 RGD:8554872
G Vps13b vacuolar protein sorting 13 homolog B JBrowse link 7 74,118,834 74,722,341 RGD:7240710
RGD:8554872
RGD:11554173
congenital stationary night blindness term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Abca4 ATP binding cassette subfamily A member 4 JBrowse link 2 225,645,539 225,783,288 RGD:8554872
G Cabp4 calcium binding protein 4 JBrowse link 1 219,383,452 219,388,009 RGD:8554872
G Cacna1f calcium voltage-gated channel subunit alpha1 F JBrowse link X 15,712,709 15,741,135 RGD:734671
RGD:8554872
RGD:13782370
RGD:11554173
G Cacna1f csnb calcium voltage-gated channel subunit alpha1 F; congenital stationary night blindness mutant RGD:13782370
G Dennd4a DENN domain containing 4A JBrowse link 8 70,293,355 70,406,675 RGD:8554872
G Gnat1 G protein subunit alpha transducin 1 JBrowse link 8 116,433,302 116,438,038 RGD:8554872
RGD:11554173
G Gnb3 G protein subunit beta 3 JBrowse link 4 157,352,558 157,359,237 RGD:11554173
G Gpr179 G protein-coupled receptor 179 JBrowse link 10 85,273,839 85,289,886 RGD:8554872
RGD:11554173
G Grk1 G protein-coupled receptor kinase 1 JBrowse link 16 81,153,489 81,165,442 RGD:8554872
G Grm6 glutamate metabotropic receptor 6 JBrowse link 10 36,345,503 36,363,416 RGD:11554173
RGD:8554872
G Lrit3 leucine-rich repeat, Ig-like and transmembrane domains 3 JBrowse link 2 235,213,017 235,232,894 RGD:8554872
RGD:11554173
G Nyx nyctalopin JBrowse link X 10,197,547 10,218,583 RGD:11554173
RGD:8554872
G Pde6b phosphodiesterase 6B JBrowse link 14 2,328,690 2,371,913 RGD:11554173
RGD:8554872
G Rho rhodopsin JBrowse link 4 147,832,136 147,837,298 RGD:11554173
RGD:8554872
G Rpgr retinitis pigmentosa GTPase regulator JBrowse link X 14,271,012 14,331,745 RGD:8554872
G Sag S-antigen visual arrestin JBrowse link 9 94,926,901 94,972,162 RGD:11554173
G Slc24a1 solute carrier family 24 member 1 JBrowse link 8 70,409,683 70,438,352 RGD:8554872
RGD:11554173
G Trpm1 transient receptor potential cation channel, subfamily M, member 1 JBrowse link 1 124,983,391 125,101,759 RGD:7175555
RGD:8554872
RGD:11554173
RGD:7183085
RGD:7183084
G Trpv3 transient receptor potential cation channel, subfamily V, member 3 JBrowse link 10 59,829,755 59,863,780 RGD:7175555
G Ush2a usherin JBrowse link 13 106,750,738 107,434,195 RGD:8554872
congenital stationary night blindness 1A term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Nyx nyctalopin JBrowse link X 10,197,547 10,218,583 RGD:7240710
RGD:8554872
congenital stationary night blindness 1B term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Grm6 glutamate metabotropic receptor 6 JBrowse link 10 36,345,503 36,363,416 RGD:7240710
RGD:8554872
G Slc24a1 solute carrier family 24 member 1 JBrowse link 8 70,409,683 70,438,352 RGD:8554872
congenital stationary night blindness 1C term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mir211 microRNA 211 JBrowse link 1 125,042,119 125,042,224 RGD:8554872
G Slc24a1 solute carrier family 24 member 1 JBrowse link 8 70,409,683 70,438,352 RGD:8554872
G Trpm1 transient receptor potential cation channel, subfamily M, member 1 JBrowse link 1 124,983,391 125,101,759 RGD:7240710
RGD:8554872
congenital stationary night blindness 1D term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Slc24a1 solute carrier family 24 member 1 JBrowse link 8 70,409,683 70,438,352 RGD:7240710
RGD:8554872
congenital stationary night blindness 1E term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gpr179 G protein-coupled receptor 179 JBrowse link 10 85,273,839 85,289,886 RGD:7240710
RGD:8554872
G Slc24a1 solute carrier family 24 member 1 JBrowse link 8 70,409,683 70,438,352 RGD:8554872
congenital stationary night blindness 1F term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Lrit3 leucine-rich repeat, Ig-like and transmembrane domains 3 JBrowse link 2 235,213,017 235,232,894 RGD:7240710
RGD:8554872
congenital stationary night blindness 1G term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gnat1 G protein subunit alpha transducin 1 JBrowse link 8 116,433,302 116,438,038 RGD:7240710
RGD:8554872
congenital stationary night blindness 1H term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cdca3 cell division cycle associated 3 JBrowse link 4 157,347,876 157,351,889 RGD:8554872
G Gnb3 G protein subunit beta 3 JBrowse link 4 157,352,558 157,359,237 RGD:8554872
RGD:7240710
Congenital Stationary Night Blindness 1I term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gucy2d guanylate cyclase 2D, retinal JBrowse link 10 55,835,695 55,851,235 RGD:7240710
RGD:8554872
congenital stationary night blindness 2A term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cacna1f calcium voltage-gated channel subunit alpha1 F JBrowse link X 15,712,709 15,741,135 RGD:7240710
RGD:8554872
Congenital Stationary Night Blindness 2B term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cabp4 calcium binding protein 4 JBrowse link 1 219,383,452 219,388,009 RGD:7240710
RGD:8554872
G Gpr152 G protein-coupled receptor 152 JBrowse link 1 219,389,418 219,394,124 RGD:8554872
congenital stationary night blindness autosomal dominant 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rho rhodopsin JBrowse link 4 147,832,136 147,837,298 RGD:7240710
RGD:8554872
congenital stationary night blindness autosomal dominant 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Pde6b phosphodiesterase 6B JBrowse link 14 2,328,690 2,371,913 RGD:7240710
RGD:8554872
congenital stationary night blindness autosomal dominant 3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gnat1 G protein subunit alpha transducin 1 JBrowse link 8 116,433,302 116,438,038 RGD:7240710
RGD:8554872
degenerative myopia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Lrp2 LDL receptor related protein 2 JBrowse link 3 55,665,153 55,822,484 RGD:13592920
G RT1-Bb RT1 class II, locus Bb JBrowse link 20 4,043,726 4,049,367 RGD:7421542
RGD:7483572
Donnai-Barrow syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Lmbrd1 LMBR1 domain containing 1 JBrowse link 9 30,939,555 31,038,381 RGD:8554872
G Lrp2 LDL receptor related protein 2 JBrowse link 3 55,665,153 55,822,484 RGD:7240710
RGD:8554872
Hamamy Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Irx5 iroquois homeobox 5 JBrowse link 19 16,415,813 16,421,088 RGD:7240710
RGD:8554872
High Myopia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Abca1 ATP binding cassette subfamily A member 1 JBrowse link 5 69,857,717 69,983,042 RGD:8554872
G Ablim2 actin binding LIM protein family, member 2 JBrowse link 14 80,044,217 80,169,491 RGD:8554872
G Aebp1 AE binding protein 1 JBrowse link 14 86,101,253 86,111,323 RGD:8554872
G Aldh1l1 aldehyde dehydrogenase 1 family, member L1 JBrowse link 4 123,516,553 123,564,067 RGD:8554872
G Anapc1 anaphase promoting complex subunit 1 JBrowse link 3 121,147,484 121,226,125 RGD:8554872
G Ankmy2 ankyrin repeat and MYND domain containing 2 JBrowse link 6 55,646,905 55,689,223 RGD:8554872
G Ap5z1 adaptor related protein complex 5 subunit zeta 1 JBrowse link 12 14,161,998 14,175,997 RGD:8554872
G Atat1 alpha tubulin acetyltransferase 1 JBrowse link 20 3,351,269 3,364,565 RGD:8554872
G Bcan brevican JBrowse link 2 187,359,674 187,373,133 RGD:8554872
G Cd109 CD109 molecule JBrowse link 8 85,951,420 86,065,411 RGD:8554872
G Ciao3 cytosolic iron-sulfur assembly component 3 JBrowse link 10 15,143,732 15,152,706 RGD:8554872
G Col17a1 collagen type XVII alpha 1 chain JBrowse link 1 267,416,681 267,465,049 RGD:8554872
G Col1a1 collagen type I alpha 1 chain JBrowse link 10 82,745,801 82,762,790 RGD:8552654
RGD:8552655
G Col2a1 collagen type II alpha 1 chain JBrowse link 7 139,454,945 139,484,403 RGD:8657342
G Cpt1b carnitine palmitoyltransferase 1B JBrowse link 7 130,395,211 130,404,731 RGD:8554872
G Crygd crystallin, gamma D JBrowse link 9 71,776,568 71,778,323 RGD:8554872
G Dut deoxyuridine triphosphatase JBrowse link 3 117,514,399 117,525,450 RGD:8554872
G Egflam EGF-like, fibronectin type III and laminin G domains JBrowse link 2 56,503,002 56,681,334 RGD:8554872
G Elavl4 ELAV like RNA binding protein 4 JBrowse link 5 130,001,387 130,144,557 RGD:8554872
G Epha8 Eph receptor A8 JBrowse link 5 155,293,731 155,321,016 RGD:8554872
G Fam160a1 family with sequence similarity 160, member A1 JBrowse link 2 184,684,851 184,993,350 RGD:8554872
G Fbn1 fibrillin 1 JBrowse link 3 117,569,708 117,766,160 RGD:8554872
G Fbn2 fibrillin 2 JBrowse link 18 53,068,495 53,272,254 RGD:8554872
G Flii FLII, actin remodeling protein JBrowse link 10 46,955,460 46,969,468 RGD:8554872
G Flrt3 fibronectin leucine rich transmembrane protein 3 JBrowse link 3 134,684,446 134,696,586 RGD:8554872
G Fuca2 alpha-L-fucosidase 2 JBrowse link 1 7,658,919 7,673,663 RGD:8554872
G Gna14 G protein subunit alpha 14 JBrowse link 1 235,165,775 235,347,986 RGD:8554872
G Grb7 growth factor receptor bound protein 7 JBrowse link 10 86,393,186 86,408,893 RGD:8554872
G Hmx2 H6 family homeobox 2 JBrowse link 1 203,515,605 203,523,266 RGD:8554872
G Hsd17b14 hydroxysteroid (17-beta) dehydrogenase 14 JBrowse link 1 101,541,266 101,551,059 RGD:8554872
G Ifit1 interferon-induced protein with tetratricopeptide repeats 1 JBrowse link 1 252,944,105 252,946,170 RGD:8554872
G Il1rap interleukin 1 receptor accessory protein JBrowse link 11 77,456,648 77,593,208 RGD:8554872
G Il36b interleukin 36, beta JBrowse link 3 1,366,123 1,464,851 RGD:8554872
G Ina internexin neuronal intermediate filament protein, alpha JBrowse link 1 266,782,835 266,794,389 RGD:8554872
G Kdr kinase insert domain receptor JBrowse link 14 34,727,677 34,787,127 RGD:8554872
G Krtap9-1 keratin associated protein 9-1 JBrowse link 10 87,759,781 87,760,576 RGD:8554872
G Lama5 laminin subunit alpha 5 JBrowse link 3 175,553,042 175,601,112 RGD:8554872
G Lgmn legumain JBrowse link 6 126,282,246 126,308,207 RGD:8554872
G Limk1 LIM domain kinase 1 JBrowse link 12 25,036,630 25,070,538 RGD:8554872
G Lrp2 LDL receptor related protein 2 JBrowse link 3 55,665,153 55,822,484 RGD:8554872
G Macrod2 mono-ADP ribosylhydrolase 2 JBrowse link 3 135,729,839 136,422,082 RGD:8554872
G Mcl1 MCL1 apoptosis regulator, BCL2 family member JBrowse link 2 197,786,212 197,788,992 RGD:8554872
G Neil2 nei-like DNA glycosylase 2 JBrowse link 15 46,371,780 46,382,730 RGD:8554872
G Nfkb1 nuclear factor kappa B subunit 1 JBrowse link 2 240,773,520 240,890,053 RGD:8554872
G Nrcam neuronal cell adhesion molecule JBrowse link 6 64,297,843 64,867,408 RGD:8554872
G Pax6 paired box 6 JBrowse link 3 95,700,241 95,728,682 RGD:8552263
RGD:8552307
RGD:8552290
G Paxbp1 PAX3 and PAX7 binding protein 1 JBrowse link 11 31,184,456 31,213,891 RGD:8554872
G Pcsk9 proprotein convertase subtilisin/kexin type 9 JBrowse link 5 126,031,368 126,053,726 RGD:8554872
G Pde6b phosphodiesterase 6B JBrowse link 14 2,328,690 2,371,913 RGD:8554872
G Pgap1 post-GPI attachment to proteins inositol deacylase 1 JBrowse link 9 61,066,170 61,134,963 RGD:8554872
G Pgs1 phosphatidylglycerophosphate synthase 1 JBrowse link 10 106,994,595 107,030,208 RGD:8554872
G Pigt phosphatidylinositol glycan anchor biosynthesis, class T JBrowse link 3 160,945,556 160,954,738 RGD:8554872
G Prkaa2 protein kinase AMP-activated catalytic subunit alpha 2 JBrowse link 5 124,568,845 124,642,569 RGD:8554872
G Prpf38b pre-mRNA processing factor 38B JBrowse link 2 211,706,245 211,715,271 RGD:8554872
G Psat1 phosphoserine aminotransferase 1 JBrowse link 1 233,124,089 233,145,941 RGD:8554872
G Ptprz1 protein tyrosine phosphatase, receptor type Z1 JBrowse link 4 49,941,046 50,140,764 RGD:8554872
G Pygm glycogen phosphorylase, muscle associated JBrowse link 1 221,756,325 221,771,142 RGD:8554872
G Rabepk Rab9 effector protein with kelch motifs JBrowse link 3 13,845,352 13,865,843 RGD:8554872
G Ralgapb Ral GTPase activating protein non-catalytic subunit beta JBrowse link 3 154,910,291 154,983,021 RGD:8554872
G Rasgrf1 RAS protein-specific guanine nucleotide-releasing factor 1 JBrowse link 8 97,277,250 97,405,095 RGD:10003136
G Rpl4 ribosomal protein L4 JBrowse link 8 69,121,682 69,126,805 RGD:8554872
G Sema3c semaphorin 3C JBrowse link 4 14,318,276 14,490,438 RGD:8554872
G Sipa1l2 signal-induced proliferation-associated 1 like 2 JBrowse link 19 58,236,201 58,399,842 RGD:8554872
G Slc22a5 solute carrier family 22 member 5 JBrowse link 10 39,201,101 39,228,090 RGD:8554872
G Slc25a25 solute carrier family 25 member 25 JBrowse link 3 11,442,396 11,476,186 RGD:8554872
G Slc28a1 solute carrier family 28 member 1 JBrowse link 1 142,948,942 142,992,410 RGD:8554872
G Slc35e2b solute carrier family 35, member E2B JBrowse link 5 173,024,335 173,050,228 RGD:8554872
G Slc6a19 solute carrier family 6 member 19 JBrowse link 1 32,199,869 32,218,628 RGD:8554872
G Sntg2 syntrophin, gamma 2 JBrowse link 6 49,123,084 49,324,530 RGD:8554872
G St14 suppression of tumorigenicity 14 JBrowse link 8 32,240,113 32,280,813 RGD:8554872
G Stac2 SH3 and cysteine rich domain 2 JBrowse link 10 85,988,367 86,004,209 RGD:8554872
G Wdr36 WD repeat domain 36 JBrowse link 18 25,637,475 25,665,801 RGD:8554872
G Zc3h13 zinc finger CCCH type containing 13 JBrowse link 15 57,340,522 57,405,287 RGD:8554872
G Zfp446 zinc finger protein 446 JBrowse link 1 65,595,518 65,608,757 RGD:8554872
G Zfp536 zinc finger protein 536 JBrowse link 1 93,689,114 94,155,457 RGD:8554872
G Zfp692 zinc finger protein 692 JBrowse link 10 43,740,739 43,752,713 RGD:8554872
High Myopia with Cataract and Vitreoretinal Degeneration term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G P3h2 prolyl 3-hydroxylase 2 JBrowse link 11 78,028,885 78,169,746 RGD:7240710
RGD:8554872
high myopia-sensorineural deafness syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Slitrk6 SLIT and NTRK-like family, member 6 JBrowse link 15 95,507,632 95,514,259 RGD:7240710
RGD:8554872
MASS Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fbn1 fibrillin 1 JBrowse link 3 117,569,708 117,766,160 RGD:7240710
RGD:8554872
multiple epiphyseal dysplasia with myopia and deafness term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Col2a1 collagen type II alpha 1 chain JBrowse link 7 139,454,945 139,484,403 RGD:7240710
RGD:8554872
Myopia 21, Autosomal Dominant term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Zfp644 zinc finger protein 644 JBrowse link 14 4,125,368 4,200,332 RGD:7240710
RGD:8554872
Myopia 22, Autosomal Dominant term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Primpol primase and DNA directed polymerase JBrowse link 16 48,863,385 48,900,409 RGD:8554872
RGD:7240710
Myopia 23, Autosomal Recessive term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Lrpap1 LDL receptor related protein associated protein 1 JBrowse link 14 80,911,281 80,923,290 RGD:7240710
RGD:8554872
Myopia 24, Autosomal Dominant term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Slc39a5 solute carrier family 39 member 5 JBrowse link 7 2,813,875 2,819,917 RGD:7240710
RGD:8554872
Myopia 25, Autosomal Dominant term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G P4ha2 prolyl 4-hydroxylase subunit alpha 2 JBrowse link 10 39,435,227 39,464,134 RGD:8554872
RGD:7240710
Myopia 26, X-Linked, Female-Limited term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Arr3 arrestin 3 JBrowse link X 70,438,590 70,452,140 RGD:8554872
RGD:7240710
Myopia 6 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ncaph2 non-SMC condensin II complex, subunit H2 JBrowse link 7 130,326,597 130,343,655 RGD:8554872
Oguchi disease-1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Sag S-antigen visual arrestin JBrowse link 9 94,926,901 94,972,162 RGD:7240710
RGD:8554872
Oguchi disease-2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Grk1 G protein-coupled receptor kinase 1 JBrowse link 16 81,153,489 81,165,442 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15610
    sensory system disease 4770
      eye disease 2339
        refractive error 168
          myopia 135
            Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction 0
            Blepharoptosis Myopia Ectopia Lentis 0
            Bornholm Eye Disease 0
            Cochlear Deafness with Myopia and Intellectual Impairment 1
            Cohen syndrome 2
            Dandy-Walker Malformation with Mental Retardation, Macrocephaly, Myopia, and Brachytelephalangy 0
            Donnai-Barrow syndrome 2
            Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness 0
            External Ophthalmoplegia and Myopia 0
            Gastrocutaneous Syndrome 0
            Hamamy Syndrome 1
            High Myopia + 77
            Isolated Microphthalmia with Corectopia 0
            MASS Syndrome 1
            Mousa Al din Al Nassar Syndrome 0
            Myopia 1 0
            Myopia 10 0
            Myopia 11 0
            Myopia 12 0
            Myopia 13 0
            Myopia 14 0
            Myopia 15 0
            Myopia 16 0
            Myopia 17, Autosomal Dominant 0
            Myopia 18, Autosomal Recessive 0
            Myopia 19, Autosomal Dominant 0
            Myopia 2 0
            Myopia 20, Autosomal Dominant 0
            Myopia 21, Autosomal Dominant 1
            Myopia 22, Autosomal Dominant 1
            Myopia 23, Autosomal Recessive 1
            Myopia 24, Autosomal Dominant 1
            Myopia 25, Autosomal Dominant 1
            Myopia 26, X-Linked, Female-Limited 1
            Myopia 27 0
            Myopia 3 0
            Myopia 5 0
            Myopia 6 1
            Myopia 7 0
            Myopia 8 0
            Myopia 9 0
            Night Blindness Skeletal Anomalies Unusual Facies 0
            Noble Bass Sherman Syndrome 0
            Polydactyly Myopia Syndrome 0
            Sinus Node Disease and Myopia 0
            Spondyloepiphyseal Dysplasia, Myopia, and Sensorineural Deafness 0
            congenital stationary night blindness + 25
            degenerative myopia 2
            high myopia-sensorineural deafness syndrome 1
            multiple epiphyseal dysplasia with myopia and deafness 1
Path 2
Term Annotations click to browse term
  disease 15610
    disease of anatomical entity 14968
      nervous system disease 10400
        sensory system disease 4770
          eye disease 2339
            refractive error 168
              myopia 135
                Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction 0
                Blepharoptosis Myopia Ectopia Lentis 0
                Bornholm Eye Disease 0
                Cochlear Deafness with Myopia and Intellectual Impairment 1
                Cohen syndrome 2
                Dandy-Walker Malformation with Mental Retardation, Macrocephaly, Myopia, and Brachytelephalangy 0
                Donnai-Barrow syndrome 2
                Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness 0
                External Ophthalmoplegia and Myopia 0
                Gastrocutaneous Syndrome 0
                Hamamy Syndrome 1
                High Myopia + 77
                Isolated Microphthalmia with Corectopia 0
                MASS Syndrome 1
                Mousa Al din Al Nassar Syndrome 0
                Myopia 1 0
                Myopia 10 0
                Myopia 11 0
                Myopia 12 0
                Myopia 13 0
                Myopia 14 0
                Myopia 15 0
                Myopia 16 0
                Myopia 17, Autosomal Dominant 0
                Myopia 18, Autosomal Recessive 0
                Myopia 19, Autosomal Dominant 0
                Myopia 2 0
                Myopia 20, Autosomal Dominant 0
                Myopia 21, Autosomal Dominant 1
                Myopia 22, Autosomal Dominant 1
                Myopia 23, Autosomal Recessive 1
                Myopia 24, Autosomal Dominant 1
                Myopia 25, Autosomal Dominant 1
                Myopia 26, X-Linked, Female-Limited 1
                Myopia 27 0
                Myopia 3 0
                Myopia 5 0
                Myopia 6 1
                Myopia 7 0
                Myopia 8 0
                Myopia 9 0
                Night Blindness Skeletal Anomalies Unusual Facies 0
                Noble Bass Sherman Syndrome 0
                Polydactyly Myopia Syndrome 0
                Sinus Node Disease and Myopia 0
                Spondyloepiphyseal Dysplasia, Myopia, and Sensorineural Deafness 0
                congenital stationary night blindness + 25
                degenerative myopia 2
                high myopia-sensorineural deafness syndrome 1
                multiple epiphyseal dysplasia with myopia and deafness 1
paths to the root

NHLBI Logo

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