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GENE - TERM ANNOTATION REPORT

RGD ID: 735108
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Serpinb6a
Name: serpin family B member 6A
Acc ID: DOID:0050439
Term: Usher syndrome
Definition: A syndrome characterized by a combination of hearing loss and visual impairment. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Usher_syndrome "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)
Serpinb6a ISOSERPINB6 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Usher syndromePMID:24033266 PMID:25741868 PMID:28492532 PMID:30311386
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