×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
CausalMutation
disease
CLINVAR
Variant discovery in patients with Mendelian vascular anomalies by next-generation sequencing and their use in patient clinical management.
28655553
2018
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
GeneticVariation
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
0.800
CausalMutation
disease
CLINVAR
Nuclear Excluded Autism-Associated Phosphatase and Tensin Homolog Mutations Dysregulate Neuronal Growth.
29373119
2018
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
GeneticVariation
disease
CLINVAR
Multiplex assessment of protein variant abundance by massively parallel sequencing.
29785012
2018
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
CausalMutation
disease
CLINVAR
Multiplex assessment of protein variant abundance by massively parallel sequencing.
29785012
2018
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
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
0.800
GeneticVariation
disease
CLINVAR
A pathogenic role for germline PTEN variants which accumulate into the nucleus.
29706633
2018
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
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
0.800
CausalMutation
disease
CLINVAR
Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome.
28677221
2017
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
GeneticVariation
disease
CLINVAR
A combination of genetic and biochemical analyses for the diagnosis of PI3K-AKT-mTOR pathway-associated megalencephaly.
28086757
2017
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
GeneticVariation
disease
CLINVAR
A retrospective chart review of the features of PTEN hamartoma tumour syndrome in children.
28526761
2017
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
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
0.800
GeneticVariation
disease
CLINVAR
Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome.
28677221
2017
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
CausalMutation
disease
CLINVAR
A retrospective chart review of the features of PTEN hamartoma tumour syndrome in children.
28526761
2017
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
CausalMutation
disease
CLINVAR
Analysis of protein-coding genetic variation in 60,706 humans.
27535533
2016
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
GeneticVariation
disease
CLINVAR
Increased PI3K/Akt activity and deregulated humoral immune response in human PTEN deficiency.
27531073
2016
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
CausalMutation
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
0.800
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
0.800
GeneticVariation
disease
CLINVAR
Analysis of protein-coding genetic variation in 60,706 humans.
27535533
2016
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
GeneticVariation
disease
CLINVAR
Cytoplasm-predominant Pten associates with increased region-specific brain tyrosine hydroxylase and dopamine D2 receptors in mouse model with autistic traits.
26579216
2015
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
CausalMutation
disease
CLINVAR
Thyroid Pathology Findings in Cowden Syndrome: A Clue for the Diagnosis of the PTEN Hamartoma Tumor Syndrome.
26185318
2015
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
GeneticVariation
disease
CLINVAR
KLLN epigenotype-phenotype associations in Cowden syndrome.
25669429
2015
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
CausalMutation
disease
CLINVAR
Cowden's syndrome with immunodeficiency.
26246517
2015
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
GeneticVariation
disease
CLINVAR
Cowden's syndrome with immunodeficiency.
26246517
2015
×
Entrez Id:
5728
Gene Symbol:
PTEN
PTEN
0.800
CausalMutation
disease
CLINVAR
Cowden Syndrome and Concomitant Pulmonary Neuroendocrine Tumor: A Presentation of Two Cases.
26798346
2015