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GENE - TERM ANNOTATION REPORT

RGD ID: 1307142
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Pls1
Name: plastin 1
Acc ID: DOID:0050564
Term: autosomal dominant nonsyndromic deafness
Definition: A nonsyndromic deafness characterized by an autosomal dominant inheritance mode. (DO)
Definition Source(s): http://ghr.nlm.nih.gov/condition/nonsyndromic-deafness "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)
Pls1 ISOPLS1 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Autosomal dominant nonsyndromic hearing impairment | ClinVar Annotator: match by term: Autosomal dominant nonsyndromic hearing lossPMID:30872814 PMID:31397523
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