×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
CausalMutation
disease
CLINVAR
First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genes.
21195604
2011
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
GeneticVariation
disease
CLINVAR
Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer.
26976419
2016
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
CausalMutation
disease
CLINVAR
Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease.
24556621
2014
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
GeneticVariation
disease
CLINVAR
Functional analysis of MUTYH mutated proteins associated with familial adenomatous polyposis.
20418187
2010
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
GeneticVariation
disease
UNIPROT
Functional analysis of MUTYH mutated proteins associated with familial adenomatous polyposis.
20418187
2010
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
CausalMutation
disease
CLINVAR
Functional analysis of MUTYH mutated proteins associated with familial adenomatous polyposis.
20418187
2010
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
CausalMutation
disease
CLINVAR
Functional characterization of human MutY homolog (hMYH) missense mutation (R231L) that is linked with hMYH-associated polyposis.
17081686
2007
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
CausalMutation
disease
CLINVAR
Functional characterization of two human MutY homolog (hMYH) missense mutations (R227W and V232F) that lie within the putative hMSH6 binding domain and are associated with hMYH polyposis.
15673720
2005
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
GeneticVariation
disease
CLINVAR
Functional characterization of two human MutY homolog (hMYH) missense mutations (R227W and V232F) that lie within the putative hMSH6 binding domain and are associated with hMYH polyposis.
15673720
2005
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
CausalMutation
disease
CLINVAR
Functional Complementation Assay for 47 MUTYH Variants in a MutY-Disrupted Escherichia coli Strain.
25820570
2015
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
GeneticVariation
disease
CLINVAR
Functional Complementation Assay for 47 MUTYH Variants in a MutY-Disrupted Escherichia coli Strain.
25820570
2015
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
GeneticVariation
disease
UNIPROT
Functional Complementation Assay for 47 MUTYH Variants in a MutY-Disrupted Escherichia coli Strain.
25820570
2015
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
GeneticVariation
disease
UNIPROT
Functional Evaluation of Nine Missense-Type Variants of the Human DNA Glycosylase Enzyme MUTYH in the Japanese Population.
26694661
2016
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
Biomarker
disease
CLINGEN
Genetic instability in lymphoblastoid cell lines expressing biallelic and monoallelic variants in the human MUTYH gene.
24569162
2014
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
GeneticVariation
disease
CLINVAR
Genetic instability in lymphoblastoid cell lines expressing biallelic and monoallelic variants in the human MUTYH gene.
24569162
2014
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
CausalMutation
disease
CLINVAR
Genetic instability in lymphoblastoid cell lines expressing biallelic and monoallelic variants in the human MUTYH gene.
24569162
2014
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
GeneticVariation
disease
CLINVAR
Genomic and functional analyses of MUTYH in Japanese patients with adenomatous polyposis.
18422726
2008
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
CausalMutation
disease
CLINVAR
Genomic variations integrated database for MUTYH-associated adenomatous polyposis.
25368107
2015
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
GeneticVariation
disease
CLINVAR
Genomic variations integrated database for MUTYH-associated adenomatous polyposis.
25368107
2015
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
GeneticVariation
disease
CLINVAR
Germline mutations but not somatic changes at the MYH locus contribute to the pathogenesis of unselected colorectal cancers.
12707038
2003
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
CausalMutation
disease
CLINVAR
Germline mutations but not somatic changes at the MYH locus contribute to the pathogenesis of unselected colorectal cancers.
12707038
2003
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
CausalMutation
disease
CLINVAR
Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis.
17489848
2007
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
GermlineCausalMutation
disease
ORPHANET
Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis.
17489848
2007
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
CausalMutation
disease
CLINVAR
Germline Mutations in the Polyposis-Associated Genes BMPR1A, SMAD4, PTEN, MUTYH and GREM1 Are Not Common in Individuals with Serrated Polyposis Syndrome.
23805267
2013
×
Entrez Id:
4595
Gene Symbol:
MUTYH
MUTYH
0.710
CausalMutation
disease
CLINVAR
Germline mutations of the MYH gene in Japanese patients with multiple colorectal adenomas.
15890374
2005