The VIM gene homepage

This database is one of the "Eye disease" gene variant databases.
General information
Gene symbol VIM
Gene name vimentin
Chromosome 10
Chromosomal band p13
Imprinted Unknown
Genomic reference NG_012413.1
Transcript reference NM_003380.3
Exon/intron information NM_003380.3 exon/intron table
Associated with diseases CTRCT30
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 15
Unique public DNA variants reported 13
Individuals with public variants 24
Hidden variants 1
Download all this gene's data Download all data
Notes This database is one of the "Eye disease" gene variant databases.
Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created March 01, 2010
Date last updated October 12, 2021
Version VIM:211012

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_003380.3.
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/VIM
HGNC 12692
Entrez Gene 7431
PubMed articles VIM
OMIM - Gene 193060
OMIM - Diseases CTRCT30 (cataract, type 30 (CTRCT-30, pulvurent))
HGMD VIM
GeneCards VIM
GeneTests VIM
Orphanet VIM


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00022604 10 vimentin NM_003380.3 NP_003371.2 15


Copyright & disclaimer
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