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Browse result for Hereditary nonpolyposis colorectal neoplasms

※ introduction

    Hereditary nonpolyposis colorectal cancer (HNPCC) is a hereditary predisposition to colon cancer. HNPCC includes (and was once synonymous with) Lynch syndrome, an autosomal dominant genetic condition that is associated with a high risk of colon cancer, endometrial cancer (second most common), ovary, stomach, small intestine, hepatobiliary tract, upper urinary tract, brain, and skin. The increased risk for these cancers is due to inherited genetic mutations that impair DNA mismatch repair. It is a type of cancer syndrome. Other HNPCC conditions include Lynch-like syndrome, polymerase proofreading-associated polyposis and familial colorectal cancer type X.

Reference
Wiki: Hereditary nonpolyposis colorectal neoplasms



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD01017P164224072
EPCAM
Epithelial cell adhesion molecule
Homo sapiens
PTMD01251P406924292
MLH1
DNA mismatch repair protein Mlh1
Homo sapiens
PTMD01653P527012956
MSH6
DNA mismatch repair protein Msh6
Homo sapiens
PTMD05126P432464436
MSH2
DNA mismatch repair protein Msh2
Homo sapiens
PTMD05575P542785395
PMS2
Mismatch repair endonuclease PMS2
Homo sapiens