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GENE - TERM ANNOTATION REPORT

RGD ID: 1560646
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Myo6
Name: myosin VI
Acc ID: DOID:0110552
Term: autosomal dominant nonsyndromic deafness 22
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/11468689 "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)
Myo6 ISOMYO6 (Homo sapiens)7240710OMIM  
Myo6 ISOMYO6 (Homo sapiens)11554173CTDCTD Direct Evidence: marker/mechanism 
Myo6 ISOMYO6 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 22 | ClinVar Annotator: match by term: DFNA 22 | ClinVar Annotator: match by term: Deafness, autosomal dominant 22 | ClinVar Annotator: match by term: Deafness, autosomal dominant nonsyndromic sensorineural 22PMID:11167014 PMID:11468689 PMID:12687499 PMID:15123708 PMID:16199547 PMID:17576681 PMID:18212818 PMID:18348273 PMID:23767834 PMID:24033266 PMID:25080041 PMID:25741868 PMID:25741877 PMID:25999546 PMID:26445815 PMID:26467025 PMID:26969326 PMID:28492532 PMID:30311386 PMID:30582396 PMID:31589614 PMID:32143290 PMID:32747562 PMID:33279834 PMID:33297549 PMID:33724713 PMID:35802133 PMID:36633841 PMID:9536098
Myo6 ISSMyo6 (Mus musculus)13592920MouseDOOMIM:606346 
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