STK11, serine/threonine kinase 11, 6794

N. diseases: 372; N. variants: 145
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1568710381
rs1568710381
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
A 0.700 CausalMutation CLINVAR [Mutation analysis of STK11 gene coding region for 20 Chinese patients with Peutz-Jeghers syndrome]. 22543132 2012
dbSNP: rs1458974438
rs1458974438
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.010 GeneticVariation BEFREE YAP overexpression in the Kras(G12D) lung cancer mouse model accelerated lung ADC progression. 26363011 2015
dbSNP: rs1458974438
rs1458974438
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.010 GeneticVariation BEFREE YAP overexpression in the Kras(G12D) lung cancer mouse model accelerated lung ADC progression. 26363011 2015
dbSNP: rs1458974438
rs1458974438
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0684249
Disease:
Carcinoma of lung
0.010 GeneticVariation BEFREE YAP overexpression in the Kras(G12D) lung cancer mouse model accelerated lung ADC progression. 26363011 2015
dbSNP: rs8111699
rs8111699
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0206081
Disease:
Hyperandrogenism
0.010 GeneticVariation BEFREE We studied the effects of a single nucleotide polymorphism (SNP) (rs8111699) in STK11 on endocrine-metabolic and body composition indexes before and after 1 year of metformin in 85 hyperinsulinemic girls with androgen excess, representing a continuum from prepuberal girls with a combined history of low birth weight and precocious pubarche over to postmenarchial girls with hyperinsulinemic ovarian hyperandrogenism. 20357370 2010
dbSNP: rs8111699
rs8111699
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0342541
Disease:
Precocious pubarche
0.010 GeneticVariation BEFREE We studied the effects of a single nucleotide polymorphism (SNP) (rs8111699) in STK11 on endocrine-metabolic and body composition indexes before and after 1 year of metformin in 85 hyperinsulinemic girls with androgen excess, representing a continuum from prepuberal girls with a combined history of low birth weight and precocious pubarche over to postmenarchial girls with hyperinsulinemic ovarian hyperandrogenism. 20357370 2010
dbSNP: rs1131690940
rs1131690940
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
0.710 GeneticVariation BEFREE We present four novel inactivating mutations identified by direct sequencing of all 9 exons of the STK11 gene in 4 patients suggestive of Peutz-Jeghers syndrome: three frameshift mutations (125-137del; 474-480del; 516-517insT) and one nonsense mutation (Q220X). 10090485 1999
dbSNP: rs1085307466
rs1085307466
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C1306459
Disease:
Primary malignant neoplasm
0.010 GeneticVariation BEFREE We predict that this novel mutation, p.Q302X, is most likely responsible for development of the PJS phenotype and may even contribute to malignancy. 22168747 2011
dbSNP: rs1085307466
rs1085307466
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0006826
Disease:
Malignant Neoplasms
0.010 GeneticVariation BEFREE We predict that this novel mutation, p.Q302X, is most likely responsible for development of the PJS phenotype and may even contribute to malignancy. 22168747 2011
dbSNP: rs1085307466
rs1085307466
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
0.010 GeneticVariation BEFREE We predict that this novel mutation, p.Q302X, is most likely responsible for development of the PJS phenotype and may even contribute to malignancy. 22168747 2011
dbSNP: rs121913315
rs121913315
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
A 0.800 CausalMutation CLINVAR Use of aromatase inhibitors in large cell calcifying sertoli cell tumors: effects on gynecomastia, growth velocity, and bone age. 25226294 2014
dbSNP: rs587778695
rs587778695
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
T 0.700 GeneticVariation CLINVAR Two variants in STK11 gene in Chinese patients with Peutz-Jeghers syndrome. 22942091 2012
dbSNP: rs1131690951
rs1131690951
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
G 0.700 CausalMutation CLINVAR Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients. 12112668 2002
dbSNP: rs137853081
rs137853081
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027651
Disease:
Neoplasms
0.020 GeneticVariation BEFREE Two LKB1/STK11 mutations were found: a missense change (Y49D) accompanied by allele loss in a cell line; and a missense change (G135R), without a detected mutation in the other allele, in a primary tumor. 10201537 1999
dbSNP: rs137853080
rs137853080
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE Two LKB1/STK11 mutations were found: a missense change (Y49D) accompanied by allele loss in a cell line; and a missense change (G135R), without a detected mutation in the other allele, in a primary tumor. 10201537 1999
dbSNP: rs786201090
rs786201090
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
T 0.700 CausalMutation CLINVAR Truncating mutations in Peutz-Jeghers syndrome are associated with more polyps, surgical interventions and cancers. 19727776 2010
dbSNP: rs730881979
rs730881979
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0206754
Disease:
Neuroendocrine Tumors
0.010 GeneticVariation BEFREE TP53 (p.R337C and p.R213*), PTEN (p.W111*, p.Q214*), CDKN2A (p.W110*), FBXW7 (p.R465H), and AKT1 (p.R23Q) were repetitive mutations found exclusively in rectal NETs, whereas SMAD4 (p.R361C) and STK11 (p.D176N) were repetitive mutations found only in gastric NETs. 30851333 2019
dbSNP: rs9282860
rs9282860
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0026769
Disease:
Multiple Sclerosis
0.010 GeneticVariation BEFREE The increased association of SNP rs9282860 in women with MS defines this variant as a genetic risk factor. 25694554 2015
dbSNP: rs1057520038
rs1057520038
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
A 0.700 GeneticVariation CLINVAR The germline mutation of LKB1 in the Peutz-Jeghers syndrome patients was identified as G215D by analyzing genomic DNA from normal lung tissue specimens. 21816872 2011
dbSNP: rs12977689
rs12977689
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE The carriers of minor allele A at rs12977689 had a higher risk of CAD compared to the homozygotes of CC (OR = 1.572, 95% CI = 1.039-2.376, <i>p</i> = 0.035), and the difference was still significant after adjustment for the other known CAD risk factors (OR' = 1.184, 95%  CI' = 1.036-1.353, <i>p</i>' = 0.013).<i>Conclusion</i>. 28349069 2017
dbSNP: rs121913315
rs121913315
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0031269
Disease:
Peutz-Jeghers Syndrome
A 0.800 CausalMutation CLINVAR Structure of the LKB1-STRAD-MO25 complex reveals an allosteric mechanism of kinase activation. 19892943 2009
dbSNP: rs1131690916
rs1131690916
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
T 0.700 GeneticVariation CLINVAR Structure of the LKB1-STRAD-MO25 complex reveals an allosteric mechanism of kinase activation. 19892943 2009
dbSNP: rs376280361
rs376280361
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
C 0.700 CausalMutation CLINVAR Structure of the LKB1-STRAD-MO25 complex reveals an allosteric mechanism of kinase activation. 19892943 2009
dbSNP: rs730881973
rs730881973
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
G 0.700 CausalMutation CLINVAR Structure of the LKB1-STRAD-MO25 complex reveals an allosteric mechanism of kinase activation. 19892943 2009
dbSNP: rs886037859
rs886037859
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
G 0.700 CausalMutation CLINVAR Structure of the LKB1-STRAD-MO25 complex reveals an allosteric mechanism of kinase activation. 19892943 2009