Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Inactivation of DNA mismatch repair by variants of uncertain significance in the PMS2 gene.
|
24027009 |
2013 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Inactivation of DNA mismatch repair by variants of uncertain significance in the PMS2 gene.
|
24027009 |
2013 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Calibration of multiple in silico tools for predicting pathogenicity of mismatch repair gene missense substitutions.
|
22949387 |
2013 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
The frequency of previously undetectable deletions involving 3' Exons of the PMS2 gene.
|
23012243 |
2013 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
The frequency of previously undetectable deletions involving 3' Exons of the PMS2 gene.
|
23012243 |
2013 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Refining the role of PMS2 in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variants.
|
23709753 |
2013 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Implementation of tumor testing for lynch syndrome in endometrial cancers at a large academic medical center.
|
23612316 |
2013 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Refining the role of PMS2 in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variants.
|
23709753 |
2013 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Yield of routine molecular analyses in colorectal cancer patients ≤70 years to detect underlying Lynch syndrome.
|
22081473 |
2012 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing.
|
22658618 |
2012 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Integrated analysis of unclassified variants in mismatch repair genes.
|
21239990 |
2011 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Pitfalls in molecular analysis for mismatch repair deficiency in a family with biallelic pms2 germline mutations.
|
21204794 |
2011 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: case series, review and follow-up guidelines.
|
21376568 |
2011 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: case series, review and follow-up guidelines.
|
21376568 |
2011 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Clinical analysis of PMS2: mutation detection and avoidance of pseudogenes.
|
20205264 |
2010 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer.
|
20487569 |
2010 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Clinical analysis of PMS2: mutation detection and avoidance of pseudogenes.
|
20205264 |
2010 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Four novel germline mutations in the MLH1 and PMS2 mismatch repair genes in patients with hereditary nonpolyposis colorectal cancer.
|
19479271 |
2009 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome.
|
18178629 |
2008 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.
|
18602922 |
2008 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.
|
18602922 |
2008 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Human PMS2 deficiency is associated with impaired immunoglobulin class switch recombination.
|
18824584 |
2008 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.
|
18602922 |
2008 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Novel biallelic mutations in MSH6 and PMS2 genes: gene conversion as a likely cause of PMS2 gene inactivation.
|
17557300 |
2007 |
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Cancer risks for mismatch repair gene mutation carriers: a population-based early onset case-family study.
|
16616355 |
2006 |