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GENE - TERM ANNOTATION REPORT

RGD ID: 3702
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Slc22a5
Name: solute carrier family 22 member 5
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)
Slc22a5 ISOSLC22A5 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Abnormality of the nervous systemPMID:20208395 PMID:20574985 PMID:21864509 PMID:24033266 PMID:25741868 PMID:28074886 PMID:28492532 PMID:30626930 PMID:31980526 PMID:32371413 PMID:32778825 PMID:34802252 PMID:35281663 PMID:36109795 PMID:36343260 PMID:37510298
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