Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation CLINVAR A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. 9428765

1998

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 GeneticVariation CLINVAR A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. 9428765

1998

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation CLINVAR Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome. 9760200

1998

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation CLINVAR STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer. 9809980

1998

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation CLINVAR Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome. 9850045

1998

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation 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
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 GeneticVariation 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
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 GeneticVariation CLINVAR Morphology-dependent resonances in a large dielectric sphere: An asymptotic calculation using local coordinates. 9908348

1992

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 GeneticVariation CLINVAR Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families. 10408777

1999

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation 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
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 GeneticVariation 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
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation 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
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation CLINVAR Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients. 12112668

2002

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation 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
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation 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
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 GeneticVariation CLINVAR Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome. 12865922

2003

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation CLINVAR Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome. 12865922

2003

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation CLINVAR Genotype-phenotype correlations in Peutz-Jeghers syndrome. 15121768

2004

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 GeneticVariation CLINVAR Relative frequency and morphology of cancers in STK11 mutation carriers. 15188174

2004

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation CLINVAR Relative frequency and morphology of cancers in STK11 mutation carriers. 15188174

2004

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation CLINVAR An LKB1 AT-AC intron mutation causes Peutz-Jeghers syndrome via splicing at noncanonical cryptic splice sites. 15608654

2005

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 GeneticVariation CLINVAR STK11 genotyping and cancer risk in Peutz-Jeghers syndrome. 15863673

2005

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation CLINVAR STK11 genotyping and cancer risk in Peutz-Jeghers syndrome. 15863673

2005

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation CLINVAR Mutations in the human LKB1/STK11 gene. 16110486

2005

Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.120 CausalMutation CLINVAR High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome. 16287113

2005