×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
A Saturation Mutagenesis Approach to Understanding PTEN Lipid Phosphatase Activity and Genotype-Phenotype Relationships.
29706350
2018
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
Multiplex assessment of protein variant abundance by massively parallel sequencing.
29785012
2018
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome.
28677221
2017
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
Immune dysregulation in patients with PTEN hamartoma tumor syndrome: Analysis of FOXP3 regulatory T cells.
27477328
2017
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability.
28475857
2017
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
GeneticVariation
disease
CLINVAR
Immune dysregulation in patients with PTEN hamartoma tumor syndrome: Analysis of FOXP3 regulatory T cells.
27477328
2017
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
Fibroblastic Polyps: A Novel Polyp Subtype in Cowden Syndrome.
29043291
2017
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
GeneticVariation
disease
CLINVAR
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
26681312
2016
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
Kinases, tails and more: regulation of PTEN function by phosphorylation.
25448482
2015
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
KLLN epigenotype-phenotype associations in Cowden syndrome.
25669429
2015
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
Malignant peripheral nerve sheath tumor in cowden syndrome: a first report.
25756585
2015
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
Functionally distinct groups of inherited PTEN mutations in autism and tumour syndromes.
25527629
2015
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
GeneticVariation
disease
CLINVAR
KLLN epigenotype-phenotype associations in Cowden syndrome.
25669429
2015
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
GeneticVariation
disease
CLINVAR
Characteristic brain magnetic resonance imaging pattern in patients with macrocephaly and PTEN mutations.
24375884
2014
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
GeneticVariation
disease
CLINVAR
A novel deleterious PTEN mutation in a patient with early-onset bilateral breast cancer.
24498881
2014
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
Second malignant neoplasms in patients with Cowden syndrome with underlying germline PTEN mutations.
24778394
2014
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
PTEN.
24905788
2014
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
Posttranslational regulation of phosphatase and tensin homolog (PTEN) and its functional impact on cancer behaviors.
25336918
2014
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
GeneticVariation
disease
CLINVAR
Second malignant neoplasms in patients with Cowden syndrome with underlying germline PTEN mutations.
24778394
2014
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
When overgrowth bumps into cancer: the PTEN-opathies.
23613428
2013
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome.
23886400
2013
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
GeneticVariation
disease
CLINVAR
High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome.
23335809
2013
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
Cowden syndrome-related mutations in PTEN associate with enhanced proteasome activity.
23475934
2013
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
Prevalence of germline PTEN, BMPR1A, SMAD4, STK11, and ENG mutations in patients with moderate-load colorectal polyps.
23399955
2013
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
1.000
CausalMutation
disease
CLINVAR
Cognitive characteristics of PTEN hamartoma tumor syndromes.
23470840
2013