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GENE - TERM ANNOTATION REPORT

RGD ID: 1308536
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Coch
Name: cochlin
Acc ID: DOID:10003
Term: sensorineural hearing loss
Definition: An inner ear disease that is characterized by hearing loss resulting from damage to the cochlea, auditory nerve and/or brainstem. (DO)
Definition Source(s): https://medlineplus.gov/ency/article/003291.htm "DO" "DO"
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)
Coch ISOCOCH (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Bilateral sensorineural hearing impairmentPMID:16261627 PMID:19461658 PMID:25780252 PMID:28492532 PMID:30311386 PMID:34652575
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