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GENE - TERM ANNOTATION REPORT

RGD ID: 1558565
Species: Mus musculus
RGD Object: Gene
Symbol: Elmod3
Name: ELMO/CED-12 domain containing 3
Acc ID: DOID:9002982
Term: Autosomal Dominant Nonsyndromic Deafness 81
Definition: Characterized by postlingual onset of slowly progressive sensorineural hearing loss. Caused by heterozygous mutation in the ELMOD3 gene on chromosome 2p11. (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)
Elmod3 ISOELMOD3 (Homo sapiens)7240710OMIM  
Elmod3 ISOELMOD3 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal dominant 81PMID:25741868 PMID:28492532 PMID:29713870
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