MSH3 gene homepage

General information
Gene symbol MSH3
Gene name mutS homolog 3
Chromosome 5
Chromosomal band q14.1
Imprinted Unknown
Genomic reference NG_016607.1
Transcript reference NM_002439.4
Associated with diseases ?, AML, cancer, gastric, CRC, Lynch Syndrome, MINAS, MRTES, polyposis, polyps, adenoma, cancer, cancer, bladder, cancer, brain, cancer, breast, cancer, endometrial, cancer, ovarian, cancer, pancreatic, cancer, rectal, cancer, skin, squamous cell carcinoma, Esophageal cancer, glioma, malignant, in silico,
Citation reference(s) -
Curators (1) John Paul Plazzer
Total number of public variants reported 0
Unique public DNA variants reported 0
Individuals with public variants 0
Hidden variants 0
Date created September 27, 2016
Date last updated November 22, 2016
Version MSH3:161122

Links to other resources
HGNC 7326
Entrez Gene 4437
PubMed articles MSH3
OMIM - Gene 600887
OMIM - Diseases AML (leukemia, myeloid, acute (AML))
cancer, gastric (cancer, gastric (neoplasm of stomach))
CRC (cancer, colorectal (CRC))
Lynch Syndrome (cancer, colorectal, nonpolyposis, hereditary, type 1 (Lynch syndrome, HNPCC-1))
MRTES (Muir-Torre Syndrome)
cancer, bladder
cancer, endometrial
cancer, ovarian
cancer, pancreatic
Esophageal cancer

Active transcripts




NCBI ID     

NCBI Protein ID     

00000014 5 mutS homolog 3 (E. coli) NM_002439.4 NP_002430.3 0

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