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GENE - TERM ANNOTATION REPORT

RGD ID: 1309271
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Kcnv2
Name: potassium voltage-gated channel modifier subfamily V member 2
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)
Kcnv2 ISOKCNV2 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Retinal dystrophyPMID:16909397 PMID:17896311 PMID:18235024 PMID:18400204 PMID:21558291 PMID:21882291 PMID:21911584 PMID:23077521 PMID:23115240 PMID:23885164 PMID:25741868 PMID:28041643 PMID:28492532 PMID:33309813 PMID:33546218
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