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GENE - TERM ANNOTATION REPORT

RGD ID: 62006
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Smc3
Name: structural maintenance of chromosomes 3
Acc ID: DOID:9004429
Term: Neurodevelopmental Disorders
Definition: These are a group of conditions with onset in the developmental period. The disorders typically manifest early in development, often before the child enters grade school, and are characterized by developmental deficits that produce impairments of personal, social, academic, or occupational functioning. (From DSM-V).
Definition Source(s): MESH:D065886
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)
Smc3 ISOSMC3 (Homo sapiens)11554173CTDCTD Direct Evidence: marker/mechanismPMID:28191889
Smc3 ISOSMC3 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Neurodevelopmental abnormality | ClinVar Annotator: match by term: Neurodevelopmental disorderPMID:25741868
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