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GENE - TERM ANNOTATION REPORT

RGD ID: 1308941
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Fscn2
Name: fascin actin-bundling protein 2, retinal
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)
Fscn2 ISOFSCN2 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Retinal dystrophyPMID:11527955 PMID:14609921 PMID:15994872 PMID:16280978 PMID:16799052 PMID:17251446 PMID:18450588 PMID:24618324 PMID:25741868 PMID:28492532 PMID:28512305
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