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VCP

Gene

valosin containing protein

HGNCHGNC:12666EnsemblENSG00000165280NCBI Gene7415
Locus: gene with protein productLocation: 9p13.3

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asIBMPFD · p97 · CDC48 · TERA
View full nomenclature history (6)
Alias symbolsIBMPFD, p97, CDC48, TERA
Previous namesvalosin-containing protein
Alias namestransitional endoplasmic reticulum ATPase

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Amyotrophic Lateral Sclerosis
Genetic Diseases, Inborn
Neurodegenerative Diseases
Cystic Fibrosis

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

AAA ATPasesVCP-Ufd1-Npl4 complex subunits

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.