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GENE - TERM ANNOTATION REPORT

RGD ID: 1309271
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Kcnv2
Name: potassium voltage-gated channel modifier subfamily V member 2
Acc ID: DOID:9006534
Term: Nervous System Malformations
Definition: Structural abnormalities of the central or peripheral nervous system resulting primarily from defects of embryogenesis.
Definition Source(s): MESH:D009421
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)
Kcnv2 ISOKCNV2 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Abnormality of the nervous systemPMID:17896311 PMID:18235024 PMID:18400204 PMID:21882291 PMID:21911584 PMID:23115240 PMID:23885164 PMID:25741868 PMID:28492532 PMID:33546218
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