VCP gene

GPTKB entity

Statements (99)
Predicate Object
gptkbp:instanceOf gptkb:gene
gptkbp:alias gptkb:CDC48
gptkb:TERA
IBMPFD
gptkbp:associatedWith gptkb:multisystem_proteinopathy
amyotrophic lateral sclerosis
inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
gptkbp:chromosomeArm p
gptkbp:discoveredBy Koller et al.
gptkbp:discoveredIn 1992
gptkbp:encodes valosin containing protein
gptkbp:Entrez_Gene_ID 7415
ENSG00000165280
gptkbp:expressedIn ubiquitous
gptkbp:fullName valosin containing protein
gptkbp:function gptkb:endoplasmic_reticulum-associated_degradation_(ERAD)
cell cycle regulation
protein degradation
autophagy
ubiquitin-dependent protein catabolic process
gptkbp:HGNC_ID 12666
https://www.w3.org/2000/01/rdf-schema#label VCP gene
gptkbp:interactsWith gptkb:ATXN3
gptkb:NSFL1C
gptkb:PLAA
gptkb:SPATA2
gptkb:UBXN10
gptkb:UBXN11
gptkb:UBXN12
gptkb:UBXN13
gptkb:UBXN14
gptkb:UBXN15
gptkb:UBXN16
gptkb:UBXN17
gptkb:UBXN18
gptkb:UBXN19
gptkb:UBXN20
gptkb:UBXN21
gptkb:UBXN22
gptkb:UBXN23
gptkb:UBXN24
gptkb:UBXN25
gptkb:UBXN26
gptkb:UBXN27
gptkb:UBXN28
gptkb:UBXN29
gptkb:UBXN2A
gptkb:UBXN2B
gptkb:UBXN30
gptkb:UBXN31
gptkb:UBXN32
gptkb:UBXN33
gptkb:UBXN34
gptkb:UBXN35
gptkb:UBXN36
gptkb:UBXN37
gptkb:UBXN38
gptkb:UBXN39
gptkb:UBXN3B
gptkb:UBXN4
gptkb:UBXN40
gptkb:UBXN41
gptkb:UBXN42
gptkb:UBXN43
gptkb:UBXN44
gptkb:UBXN45
gptkb:UBXN46
gptkb:UBXN47
gptkb:UBXN48
gptkb:UBXN49
gptkb:UBXN5
gptkb:UBXN50
gptkb:UBXN6
gptkb:UBXN8
gptkb:UBXN9
gptkb:FAF1
gptkb:UBXN7
gptkb:YOD1
gptkb:Derlin-1
gptkb:NPL4
gptkb:UFD1L
gptkb:UBXN1
p47
gptkbp:length 17 exons
gptkbp:locatedOnChromosome 9
9p13.3
gptkbp:mutationAssociatedWith causes Paget disease of bone
causes frontotemporal dementia
causes inclusion body myopathy
causes multisystem proteinopathy
gptkbp:OMIM 601023
gptkbp:organism gptkb:Homo_sapiens
gptkbp:orthologInMouse Vcp
gptkbp:orthologInYeast gptkb:CDC48
gptkbp:proteinFamily gptkb:AAA_ATPase_family
gptkbp:UniProtID gptkb:P55072
gptkbp:bfsParent gptkb:VCP
gptkb:p97/VCP
gptkbp:bfsLayer 7