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GENE - TERM ANNOTATION REPORT

RGD ID: 3135
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Myo1a
Name: myosin IA
Acc ID: DOID:0110571
Term: autosomal dominant nonsyndromic deafness 48
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with progressive hearing loss and has_material_basis_in variation in the chromosome region 12q13-q14. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/12736868 "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)
Myo1a ISOMYO1A (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal dominant 48PMID:12736868 PMID:24033266 PMID:24616153 PMID:25741868
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