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GENE - TERM ANNOTATION REPORT

RGD ID: 1310462
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Rdh12
Name: retinol dehydrogenase 12
Acc ID: DOID:8501
Term: fundus dystrophy
Definition: A group of disorders involving predominantly the posterior portion of the ocular fundus, due to degeneration in the sensory layer of the RETINA; RETINAL PIGMENT EPITHELIUM; BRUCH MEMBRANE; CHOROID; or a combination of these tissues.
Definition Source(s): MESH:D058499
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
Rdh12 ISORDH12 (Homo sapiens)11554173CTDCTD Direct Evidence: marker/mechanismPMID:18048336
Rdh12 ISORDH12 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Retinal dystrophyPMID:15258582 PMID:15322982 PMID:16199547 PMID:16269441 PMID:17389517 PMID:17512964 PMID:17576681 PMID:17964524 PMID:18779497 PMID:19011012 PMID:19140180 PMID:20301475 PMID:20683928 PMID:20736127 PMID:21151602 PMID:22065924 PMID:23591405 PMID:23661369 PMID:23847139 PMID:23900199 PMID:24265693 PMID:24474277 PMID:24625443 PMID:24752437 PMID:25133751 PMID:25412400 PMID:25494902 PMID:25741868 PMID:25910913 PMID:26047050 PMID:26103963 PMID:26261414 PMID:26306921 PMID:26497376 PMID:26667666 PMID:26848971 PMID:26992781 PMID:27032803 PMID:27208204 PMID:27809489 PMID:28041643 PMID:28492532 PMID:28559085 PMID:29178642 PMID:29186038 PMID:30134391 PMID:30372751 PMID:30543658 PMID:30718709 PMID:30902645 PMID:30979730 PMID:31456290 PMID:32014858 PMID:32141364 PMID:32322264 PMID:32790509 PMID:33090715 PMID:33576794 PMID:34001834 PMID:34448047 PMID:35994252 PMID:36284670 PMID:36690427 PMID:36909829 PMID:9536098
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