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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + MSH2  Accession Numbers +
Approved Name + mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli) U03911 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:7325 Mouse Genome Database ID +
Status + Approved MGI:101816 MGD ID 
Chromosome + 2p21 Rat Genome Database ID (mapped data supplied by RGD) +
Previous Symbols + COCA1 RGD:620786 RGD ID 
Previous Names + "mutS (E. coli) homolog 2 (colon cancer, nonpolyposis type 1)" Entrez Gene ID +
Aliases + HNPCC, HNPCC1 4436 Gene  Map Viewer 
Name Aliases +   CCDS IDs +
Locus Type + gene with protein product CCDS1834.1 CCDS ID 
  Pubmed IDs +
Gene Symbol Links 8484120, 9843200 PMID  CiteXplore 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
VEGA IDs +
OTTHUMG00000128861 VEGA GeneView 
Ensembl ID (mapped data supplied by Ensembl) +
ENSG00000095002 Ensembl GeneView  UCSC 
Specialist Database Links RefSeq (mapped data supplied by NCBI) +
COSMIC Orphanet:123487
 
NM_000251 GenBank EMBL DDBJ UCSC
OMIM ID (mapped data supplied by NCBI) +
Locus Specific Database Links 609309 OMIM 
Hereditary Non-Polyposis Colorectal Cancer, HNPCC,
Mismatch Repair Genes Variant Database,
Colon cancer gene variant databases,
Zhejiang University Center for Genetic and Genomic Medicine,
LOVD - Leiden Open Variation Database
 
UCSC ID (mapped data supplied by UCSC) +
uc002rvy.1 UCSC Index 
UniProt ID (mapped data supplied by UniProt) +
  P43246 UniProt  UCSC 

See Column definitions for descriptions of the various data fields. Also see our custom downloads page for bulk access to our data

 


The work of the HGNC is supported by NHGRI grant P41 HG003345, the UK Medical Research Council and the Wellcome Trust.