Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 Biomarker disease BEFREE Phosphatase and tensin homolog on chromosome 10 (PTEN) is a tumor suppressor and autism-associated gene that exerts an important influence over neuronal structure and function during development. 31240311 2020
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease BEFREE Conformational Dynamics and Allosteric Regulation Landscapes of Germline PTEN Mutations Associated with Autism Compared to Those Associated with Cancer. 31006514 2019
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease BEFREE This regional and WM enlargement recapitulates structural abnormalities found in individuals with PTEN haploinsufficiency and autism. 31804455 2019
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease BEFREE Our results lend insight into distinctive structural effects of germline PTEN mutations associated with PTEN-ASD vs. those associated with PTEN-cancer, potentially aiding in identification of the shared and separate molecular features that contribute to autism or cancer, thus, providing a deeper understanding of genotype-phenotype relationships for germline PTEN mutations. 29663862 2019
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 Biomarker disease BEFREE To investigate PTEN's role during neurodevelopment and its implication for autism, several conditional <i>Pten</i> knockout mouse models have been generated. 31427284 2019
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease BEFREE A novel mutation in the PTEN gene was identified in a 16-year-old girl with autism, mental retardation, language delay, extreme macrocephaly (+4.7SD) with a prominent forehead, and digital minor anomalies. 28774669 2018
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease BEFREE In addition, autistic phenotypes are found in 10-20% of individuals carrying the germline PTEN mutation with macrocephaly. 29608813 2018
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease BEFREE Germline mutations in the tumor-suppressor gene PTEN predispose to subsets of Cowden syndrome (CS), Bannayan-Riley-Ruvalcaba syndrome, and autism. 28677221 2017
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease BEFREE Especially useful would be an algorithm for predicting the impact of nonsynonymous single-nucleotide polymorphisms in the gene for PTEN, a protein that is implicated in most human cancers and connected to germline disorders that include autism. 27310656 2016
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 Biomarker disease BEFREE Reciprocal regulation of autism-related genes MeCP2 and PTEN via microRNAs. 26843422 2016
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease BEFREE Molecular and phenotypic abnormalities in individuals with germline heterozygous PTEN mutations and autism. 25288137 2015
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease BEFREE The phenotypic spectrum of PTEN mutations expanded to include autism with macrocephaly only 10 years ago. 25916396 2015
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease BEFREE Our work implies that alleles causing incomplete loss of PTEN function are more commonly linked to autism than to severe PHTS cases. 25527629 2015
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 Biomarker disease BEFREE Variants of human PTEN linked to somatic cancers and disorders on the autism spectrum are shown to be impaired in their conformational stability, catalytic activity, or both. 25647146 2015
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 Biomarker disease BEFREE Exome sequencing of the family also identified a rare inherited variant predicted to disrupt splicing of TPTE / PTEN2, a PTEN homologue, which may likewise contribute to both macrocephaly and autism risk. 26076356 2015
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 Biomarker disease BEFREE Autism-epilepsy phenotype with macrocephaly suggests PTEN, but not GLIALCAM, genetic screening. 24580998 2014
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease BEFREE De novo phosphatase and tensin homolog on chromosome ten (PTEN) mutations are a cause of sporadic autism. 24145404 2013
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease BEFREE PHTS patients with destabilizing PTEN mutations and proteasome hyperactivity are more susceptible to develop neurologic symptoms such as mental retardation and autism than mutation-positive patients with normal proteasome activity. 23475934 2013
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 AlteredExpression disease BEFREE GABRB3, RELN, and HTR2A showed reduced expression, whereas CD38, ITGB3, MAOA, MECP2, OXTR, and PTEN showed elevated expression in autism. 22030357 2012
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease BEFREE In addition, emerging data suggest that PTEN mutation can synergize with mutations in other autism susceptibility genes to contribute to the development of autistic behaviors. 22664040 2012
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease CLINVAR Estimate of de novo mutation frequency in probands with PTEN hamartoma tumor syndrome. 22595938 2012
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease CLINVAR Lifetime cancer risks in individuals with germline PTEN mutations. 22252256 2012
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease BEFREE Phosphatase and tensin homolog (PTEN) gene mutations and autism: literature review and a case report of a patient with Cowden syndrome, autistic disorder, and epilepsy. 21960672 2012
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 GeneticVariation disease BEFREE Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly. 20533527 2010
Entrez Id: 5728
Gene Symbol: PTEN
PTEN
0.500 Biomarker disease CTD_human Novel PTEN mutations in neurodevelopmental disorders and macrocephaly. 18759867 2009