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GENE - TERM ANNOTATION REPORT

RGD ID: 70928
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Kif1c
Name: kinesin family member 1C
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)
Kif1c ISOKIF1C (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Hereditary spastic paraplegiaPMID:17576681 PMID:24482476 PMID:25741868 PMID:26633545 PMID:28492532 PMID:28832565 PMID:29482223 PMID:9536098
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