The VCL gene homepage

General information
Gene symbol VCL
Gene name vinculin
Chromosome 10
Chromosomal band q22.1-q23
Imprinted Unknown
Genomic reference LRG_383
Transcript reference NM_014000.2
Exon/intron information NM_014000.2 exon/intron table
Associated with diseases CMD1W, CMH15
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 471
Unique public DNA variants reported 255
Individuals with public variants 53
Hidden variants 11
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated February 26, 2024
Version VCL:240226

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_014000.2.
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 http://www.LOVD.nl/VCL
HGNC 12665
Entrez Gene 7414
PubMed articles VCL
OMIM - Gene 193065
OMIM - Diseases CMD1W (cardiomyopathy, dilated, type 1W (CMD-1W))
CMH15 (cardiomyopathy, hypertrophic, familial, type 15 (CMH-15))
HGMD VCL
GeneCards VCL
GeneTests VCL
Orphanet VCL


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00024148 10 transcript variant 1 NM_014000.2 NP_054706.1 471


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