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GENE - TERM ANNOTATION REPORT

RGD ID: 1596713
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Rp1
Name: RP1, axonemal microtubule associated
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)
Rp1 ISORP1 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Retinal dystrophyPMID:10391211 PMID:10391212 PMID:10401003 PMID:11095597 PMID:11139241 PMID:11317367 PMID:11527933 PMID:11694261 PMID:12764676 PMID:15183808 PMID:15933747 PMID:15994872 PMID:16185528 PMID:1783394 PMID:19933189 PMID:20664799 PMID:22334370 PMID:23049240 PMID:23105016 PMID:23424971 PMID:23991373 PMID:24033266 PMID:24339724 PMID:25097241 PMID:25494902 PMID:25692139 PMID:25698705 PMID:25741868 PMID:26355662 PMID:27160483 PMID:27208204 PMID:27391102 PMID:27623337 PMID:28041643 PMID:28076437 PMID:28492532 PMID:29068140 PMID:29425069 PMID:29641573 PMID:29785639 PMID:29847639 PMID:30027431 PMID:30718709 PMID:30731082 PMID:30913292 PMID:31047384 PMID:31054281 PMID:31213501 PMID:31253780 PMID:31456290 PMID:32100970 PMID:32193659 PMID:32562694 PMID:32565670 PMID:32783370 PMID:33090715 PMID:33546218 PMID:33576794 PMID:33681214 PMID:33946315 PMID:34073704 PMID:34721897 PMID:34906470 PMID:36284460 PMID:36909829 PMID:8931712
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