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GENE - TERM ANNOTATION REPORT

RGD ID: 731621
Species: Homo sapiens
RGD Object: Gene
Symbol: VCP
Name: valosin containing protein
Acc ID: DOID:607
Term: paraplegia
Definition: Severe or complete loss of motor function in the lower extremities and lower portions of the trunk. This condition is most often associated with SPINAL CORD DISEASES, although BRAIN DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; NEUROMUSCULAR DISEASES; and MUSCULAR DISEASES may also cause bilateral leg weakness.
Definition Source(s): MESH:D010264
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)
VCP IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Spastic paraplegiaPMID:15034582 PMID:18845250 PMID:20604808 PMID:22270372 PMID:22909335 PMID:23333620 PMID:25617006 PMID:25741868 PMID:28492532 PMID:33144514
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