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GENE - TERM ANNOTATION REPORT

RGD ID: 1343693
Species: Homo sapiens
RGD Object: Gene
Symbol: MYO15A
Name: myosin XVA
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)
MYO15A IAGP 1600554RGDDFNB3, OMIM:600316, DNA:point mutation:exon:I892F 
MYO15A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Congenital sensorineural hearing impairmentPMID:17546645 PMID:24033266 PMID:24875298 PMID:25741868 PMID:26969326 PMID:28492532 PMID:32860223
MYO15A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Congenital sensorineural hearing impairmentPMID:25741868
MYO15A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Congenital sensorineural hearing impairmentPMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098
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