Return To The Previous Page
Buy a Package
Number Of Visible Items Remaining : 3 Item

Genetic mutations that are associated with an increased risk of colorectal cancer

Genetic mutations that are associated with an increased risk of colorectal cancer
Syndrome/disease Responsible gene Mode of acquisition
FAP APC Germline (inherited)
HNPCC (Lynch syndrome) MMR genes
hMSH2
hMLH1
hPMS1
hPMS2
hMSH3
hMSH6
EPCAM (epigenetic alteration)
Sporadic tumor Tumor suppressor genes Somatic (acquired)
TP53
DCC
APC
Oncogenes
MYC
RAS
SRC
HER2
MMR genes (epigenetic change)
FAP: familial adenomatous polyposis; APC: adenomatous polyposis coli gene; HNPCC: hereditary nonpolyposis colorectal cancer; MMR: mismatch repair; hMSH: human mutS homolog; hMLH1: human mutL homolog 1; hPMS: human postmeiotic segregation; EPCAM: epithelial cell adhesion molecule; DCC: deleted in colorectal carcinoma; HER2: human epidermal growth factor receptor 2.
Graphic 60613 Version 7.0

Do you want to add Medilib to your home screen?