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GENE - TERM ANNOTATION REPORT

RGD ID: 13953559
Species: Sus scrofa
RGD Object: Gene
Symbol: SLC6A1
Name: solute carrier family 6 member 1
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)
SLC6A1 ISOSLC6A1 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Neurodevelopmental disorderPMID:25741868 PMID:27541642 PMID:28492532
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