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GENE - TERM ANNOTATION REPORT

RGD ID: 621648
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Fdxr
Name: ferredoxin reductase
Acc ID: DOID:9003451
Term: Auditory Neuropathy and Optic Atrophy
Definition: An autosomal recessive neurologic disorder characterized by onset of visual and hearing impairment in the first or second decades. (OMIM)
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)
Fdxr ISOFDXR (Homo sapiens)7240710OMIM  
Fdxr ISOFDXR (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: AUDITORY NEUROPATHY AND OPTIC ATROPHY | ClinVar Annotator: match by term: FDXR-related conditionPMID:24033266 PMID:25741868 PMID:28492532 PMID:28965846 PMID:29040572 PMID:30250212 PMID:6766943
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