×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
Biomarker
group
MGD
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
Biomarker
group
MGD
×
Entrez Id:
4072
Gene Symbol:
EPCAM
EPCAM
0.410
GeneticVariation
group
CLINVAR
×
Entrez Id:
1495
Gene Symbol:
CTNNA1
CTNNA1
0.300
Biomarker
group
CLINGEN
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.640
CausalMutation
group
CLINVAR
"""Central arousal"" and sexual responsiveness in the snail, Helix aspersa."
2059188
1991
×
Entrez Id:
80204
Gene Symbol:
FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
"""Central arousal"" and sexual responsiveness in the snail, Helix aspersa."
2059188
1991
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
GeneticVariation
group
CLINVAR
"""Null pattern"" of immunoreactivity in a Lynch syndrome-associated colon cancer due to germline MSH2 mutation and somatic MLH1 hypermethylation."
22067334
2011
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
GeneticVariation
group
LHGDN
A 10-Mb paracentric inversion of chromosome arm 2p inactivates MSH2 and is responsible for hereditary nonpolyposis colorectal cancer in a North-American kindred.
12203789
2002
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
0.640
CausalMutation
group
CLINVAR
A case of early onset rectal cancer of Lynch syndrome with a novel deleterious PMS2 mutation.
26232782
2015
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
Biomarker
group
CTD_human
A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1.
20020535
2010
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1.
20020535
2010
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.640
CausalMutation
group
CLINVAR
A cohort analysis of men with a family history of BRCA1/2 and Lynch mutations for prostate cancer.
27456091
2016
×
Entrez Id:
80204
Gene Symbol:
FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
A cohort analysis of men with a family history of BRCA1/2 and Lynch mutations for prostate cancer.
27456091
2016
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
Biomarker
group
CTD_human
A CRM1-dependent nuclear export pathway is involved in the regulation of MutLα subcellular localization.
21064154
2011
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
A founder MLH1 mutation in families from the districts of Modena and Reggio-Emilia in northern Italy with hereditary non-polyposis colorectal cancer associated with protein elongation and instability.
14985405
2004
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
A founder MLH1 mutation in Lynch syndrome families from Piedmont, Italy, is associated with an increased risk of pancreatic tumours and diverse immunohistochemical patterns.
24802709
2014
×
Entrez Id:
22909
Gene Symbol:
FAN1
FAN1
0.300
Biomarker
group
CLINGEN
A genetic screen identifies FAN1, a Fanconi anemia-associated nuclease necessary for DNA interstrand crosslink repair.
20603073
2010
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
GeneticVariation
group
CLINVAR
A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome.
15235030
2004
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome.
15235030
2004
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
GeneticVariation
group
CLINVAR
A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic setting.
18625694
2008
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.640
GeneticVariation
group
LHGDN
A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic setting.
18625694
2008
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.640
CausalMutation
group
CLINVAR
A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic setting.
18625694
2008
×
Entrez Id:
80204
Gene Symbol:
FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic setting.
18625694
2008
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
0.640
CausalMutation
group
CLINVAR
A homozygote splice site PMS2 mutation as cause of Turcot syndrome gives rise to two different abnormal transcripts.
19039682
2009
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
0.640
GeneticVariation
group
CLINVAR
A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotype.
25691505
2015