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RGD ID: 1305446
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Trrap
Name: transformation/transcription domain-associated protein
Acc ID: DOID:0112166
Term: autosomal dominant nonsyndromic deafness 75
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the TRRAP gene on chromosome 7q22.1. (DO)
Definition Source(s): "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)
Trrap ISOTRRAP (Homo sapiens)7240710OMIM  
Trrap ISOTRRAP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Deafness, autosomal dominant 75PMID:25741868 PMID:28492532 PMID:31231791
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