The MSH6 gene homepage

General information
Gene symbol MSH6
Gene name mutS homolog 6
Chromosome 2
Chromosomal band p16
Imprinted Unknown
Genomic reference LRG_219
Transcript reference NM_000179.2
Associated with diseases ENDOMETRIAL CANCER, LYNCH5, MMRCS3
Citation reference(s) -
Curators (2) Florian Bayersdorfer and Sabine Heber
Total number of public variants reported 12
Unique public DNA variants reported 11
Individuals with public variants 0
Hidden variants -
Date created July 08, 2016
Date last updated July 17, 2023
Version MSH6:230717

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
HGNC 7329
Entrez Gene 2956
PubMed articles MSH6
OMIM - Gene 600678
OMIM - Diseases ENDOMETRIAL CANCER
LYNCH5 (LYNCH SYNDROME 5)
MMRCS3 (MISMATCH REPAIR CANCER SYNDROME 3)
HGMD MSH6
GeneCards MSH6
GeneTests MSH6


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000013 2 mutS homolog 6 (E. coli), transcript variant 1 NM_000179.2 NP_000170.1 12


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