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GENE - TERM ANNOTATION REPORT

RGD ID: 628608
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Slc16a2
Name: solute carrier family 16 member 2
Acc ID: DOID:2476
Term: hereditary spastic paraplegia
Definition: A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Familial_spastic_paraplegia "DO" "DO"
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)
Slc16a2 ISOSLC16A2 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Hereditary spastic paraplegiaPMID:18414213 PMID:20301789 PMID:23568789 PMID:24265446 PMID:24721225 PMID:25527620 PMID:25741868 PMID:27212794 PMID:28492532 PMID:28832565
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