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GENE - TERM ANNOTATION REPORT

RGD ID: 69337
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Trpv4
Name: transient receptor potential cation channel, subfamily V, member 4
Acc ID: DOID:9005801
Term: Diets-Jongmans Syndrome
Definition: An autosomal dominant disorder characterized by mild to moderately impaired intellectual development with a recognizable facial gestalt. Caused by heterozygous mutation in the KDM3B gene on chromosome 5q31. (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)
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