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VCP - valosin containing protein
- Synonym(s) : CDC48, IBMPFD, p97, TERA, transitional endoplasmic reticulum ATPase
- Previous symbols and names : Valosin-containing protein, valosin-containing protein
- Type : gene with protein product
- Chromosomal location : 9p13.3
- OMIM: 601023
- HGNC: 12666
- UniProtKB: P55072
- Genatlas: VCP
- GenCC: VCP
- Ensembl: ENSG00000165280
- IUPHAR-DB: -
- Reactome: P55072
- LOVD: VCP
Diseases list
- Disease-causing germline mutation(s) in Adult-onset distal myopathy due to VCP mutation
ORPHA:329478 
- Disease-causing germline mutation(s) in Amyotrophic lateral sclerosis
ORPHA:803 - Disease-causing germline mutation(s) in Autosomal dominant Charcot-Marie-Tooth disease type 2Y
ORPHA:435387 - Disease-causing germline mutation(s) in Frontotemporal dementia with motor neuron disease
ORPHA:275872 - Disease-causing germline mutation(s) in Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
ORPHA:52430 - Disease-causing germline mutation(s) in Spastic paraplegia-Paget disease of bone syndrome
ORPHA:329475 - Major susceptibility factor in Behavioral variant of frontotemporal dementia
ORPHA:275864 - Major susceptibility factor in Progressive non-fluent aphasia
ORPHA:100070
: AssessedAdditional information
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