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GENE - TERM ANNOTATION REPORT

RGD ID: 737151
Species: Homo sapiens
RGD Object: Gene
Symbol: SCN9A
Name: sodium voltage-gated channel alpha subunit 9
Acc ID: DOID:9005687
Term: Autosomal Dominant Intellectual Developmental Disorder 64
Definition: Characterized by mildly to severely impaired intellectual development (ID) with speech delays. Caused by heterozygous mutation in the ZNF292 gene on chromosome 6q14.
Definition Source(s): OMIM:619188
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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