The MSH2 gene homepage

General information
Gene symbol MSH2
Gene name mutS homolog 2
Chromosome 2
Chromosomal band p21
Imprinted Unknown
Genomic reference LRG_218
Transcript reference NM_000251.2
Associated with diseases HNPCC-1, MMRCS, MRTES
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 77
Unique public DNA variants reported 13
Individuals with public variants 35
Hidden variants 1
Date created November 30, -0001
Date last updated September 28, 2016
Version MSH2:160928

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
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
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:7325
Entrez Gene 4436
PubMed articles MSH2
OMIM - Gene 609309
OMIM - Diseases HNPCC-1 (Lynch)
MMRCS (cancer syndrome, mismatch repair (MMRCS))
MRTES (Muir-Torre syndrome (MRTES))


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00012858 2 transcript variant 1 NM_000251.2 NP_000242.1 77