The VCP gene homepage

This database is one of the gene variant databases from the "Leiden Muscular Dystrophy pages" (LMDp).
General information
Gene symbol VCP
Gene name valosin containing protein
Chromosome 9
Chromosomal band p13
Imprinted Unknown
Genomic reference NG_007887.1
Transcript reference NM_007126.3
Exon/intron information NM_007126.3 exon/intron table
Associated with diseases ALS14, CMT2Y, IBMPFD
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Johan den Dunnen
Total number of public variants reported 202
Unique public DNA variants reported 84
Individuals with public variants 306
Hidden variants 9
Download all this gene's data Download all data
Notes This database is one of the gene variant databases from the "Leiden Muscular Dystrophy pages" (LMDp).
Date created March 01, 2010
Date last updated September 05, 2022
Version VCP:220905

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_007126.3.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/VCP
HGNC 12666
Entrez Gene 7415
PubMed articles VCP
OMIM - Gene 601023
OMIM - Diseases ALS14 (sclerosis, lateral, amyotrophic, type 14, with/without frontotemporal dementia (ALS14))
CMT2Y (Charcot-Marie-Tooth disease, type 2Y)
IBMPFD (myopathy, inclusion body, with early-onset Paget disease and frontotemporal dementia (IBMPFD))
HGMD VCP
GeneCards VCP
GeneTests VCP
Orphanet VCP


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00022574 9 valosin containing protein NM_007126.3 NP_009057.1 202


Copyright & disclaimer
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