
MLH1 - Wikipedia
DNA mismatch repair protein Mlh1 or MutL protein homolog 1 is a protein that in humans is encoded by the MLH1 gene located on chromosome 3. The gene is commonly associated with …
About Mutations in the MLH1 Gene - Memorial Sloan Kettering Cancer Center
Jul 12, 2023 · If you both have a mutation in the MLH1 gene, there’s a chance your child could be born with a rare but serious condition called Constitutional Mismatch Repair Deficiency …
MLH1 gene: MedlinePlus Genetics
The MLH1 gene provides instructions for making a protein that plays an essential role in repairing DNA. This protein helps fix errors that are made when DNA is copied (DNA replication) in …
Gene Mutation MLH1 and Cancer Risk - Everyday Health
Aug 23, 2022 · An error, or mutation, in one copy of the MLH1 gene is one of the causes of Lynch syndrome, an inherited disorder that raises a person’s risk of developing colorectal cancer and …
MLH1 - MyPathologyReport.ca
MLH1 is a gene that produces a protein involved in DNA repair, specifically in a process called mismatch repair. This protein works closely with other mismatch repair proteins, including …
Cancer Treatment in People with an MLH1 Mutation
Aug 29, 2024 · People with Lynch syndrome due to an MLH1 mutation may have different options for cancer treatment. Learn about the treatment options for people with mutations in this gene.
MLH1 Gene Mutations (Lynch Syndrome): Risks and Options
Sep 6, 2024 · Read about the latest expert guidelines for cancer screening and prevention for people with an MLH1 mutation. Learn about research studies enrolling high-risk patients.
Identification of Lynch syndrome mutations in the MLH1-PMS2 …
Missense alterations of the mismatch repair gene MLH1 have been identified in a significant proportion of individuals suspected of having Lynch syndrome, a hereditary syndrome which …
MLH1 Gene - GeneCards | MLH1 Protein | MLH1 Antibody
Dec 25, 2024 · MLH1 (MutL Homolog 1) is a Protein Coding gene. Diseases associated with MLH1 include Mismatch Repair Cancer Syndrome 1 and Lynch Syndrome 2. Among its …
Lynch syndrome, molecular mechanisms and variant classification
LS patients carry germline loss of function (LoF) variants in one of the four key genes involved in MMR: MutL homolog 1 (MLH1), MutS homolog 2 (MSH2), postmeiotic segregation increased 2 …