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GENE - TERM ANNOTATION REPORT

RGD ID: 620499
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Impg1
Name: interphotoreceptor matrix proteoglycan 1
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)
Impg1 ISOIMPG1 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Retinal dystrophyPMID:17576681 PMID:23993198 PMID:25741868 PMID:28492532 PMID:28644393 PMID:30215852 PMID:30688845 PMID:30902645 PMID:3196484 PMID:32531858 PMID:32817297 PMID:9536098
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