The LIM2 gene homepage

This database is one of the "Eye disease" gene variant databases.
General information
Gene symbol LIM2
Gene name lens intrinsic membrane protein 2, 19kDa
Chromosome 19
Chromosomal band q13.4
Imprinted Unknown
Genomic reference NC_000019.9
Transcript reference NM_001161748.1, NM_030657.3
Exon/intron information NM_001161748.1 exon/intron table
Associated with diseases CTRCT, CTRCT19
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 18
Unique public DNA variants reported 17
Individuals with public variants 13
Hidden variants -
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 April 16, 2023
Version LIM2:230416

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_001161748.1.
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/LIM2
HGNC 6610
Entrez Gene 3982
PubMed articles LIM2
OMIM - Gene 154045
OMIM - Diseases CTRCT19 (cataract, type 19)
HGMD LIM2
GeneCards LIM2
GeneTests LIM2
Orphanet LIM2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00011140 19 transcript variant 1 NM_030657.3 NP_085915.2 18
00025824 19 transcript variant 2 NM_001161748.1 NP_001155220.1 14


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