Gene: STK11 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 GeneticVariation group CLINVAR Morphology-dependent resonances in a large dielectric sphere: An asymptotic calculation using local coordinates. 9908348 1992
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome. 9760200 1998
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. 9428765 1998
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome. 9850045 1998
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 GeneticVariation group CLINVAR A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. 9428765 1998
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer. 9809980 1998
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer. 9887330 1999
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 GeneticVariation group CLINVAR Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer. 9887330 1999
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 GeneticVariation group CLINVAR Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families. 10408777 1999
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR Somatic mutations in the STK11/LKB1 gene are uncommon in rare gynecological tumor types associated with Peutz-Jegher's syndrome. 10623683 2000
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 GeneticVariation group CLINVAR Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma. 11389158 2001
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma. 11389158 2001
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients. 12112668 2002
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients. 12372054 2002
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 GeneticVariation group CLINVAR Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome. 12865922 2003
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome. 12865922 2003
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 GeneticVariation group BEFREE LKB1 is a serine-threonine protein kinase mutated in patients with an autosomal dominantly inherited cancer syndrome predisposing to multiple benign and malignant tumours, termed Peutz-Jeghers syndrome. 12829253 2003
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR Functional analysis of LKB1/STK11 mutants and two aberrant isoforms found in Peutz-Jeghers Syndrome patients. 12552571 2003
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 GeneticVariation group CLINVAR Relative frequency and morphology of cancers in STK11 mutation carriers. 15188174 2004
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR Relative frequency and morphology of cancers in STK11 mutation carriers. 15188174 2004
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR Genotype-phenotype correlations in Peutz-Jeghers syndrome. 15121768 2004
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome. 16287113 2005
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 GeneticVariation group CLINVAR STK11 genotyping and cancer risk in Peutz-Jeghers syndrome. 15863673 2005
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR Mutations in the human LKB1/STK11 gene. 16110486 2005
Entrez Id: 6794
Gene Symbol: STK11
STK11 		0.120 CausalMutation group CLINVAR An LKB1 AT-AC intron mutation causes Peutz-Jeghers syndrome via splicing at noncanonical cryptic splice sites. 15608654 2005