PTEN Chromosome 10

Phosphatase and tensin homolog
1069 variants 1069 Health Risk

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What This Gene Does
This gene was identified as a tumor suppressor that is mutated in a large number of cancers at high frequency. The protein encoded by this gene is a phosphatidylinositol-3,4,5-trisphosphate 3-phosphatase. It contains a tensin like domain as well as a catalytic domain similar to that of the dual specificity protein tyrosine phosphatases. Unlike most of the protein tyrosine phosphatases, this protein preferentially dephosphorylates phosphoinositide substrates. It negatively regulates intracellular levels of phosphatidylinositol-3,4,5-trisphosphate in cells and functions as a tumor suppressor by negatively regulating AKT/PKB signaling pathway. The use of a non-canonical (CUG) upstream initiation site produces a longer isoform that initiates translation with a leucine, and is thought to be preferentially associated with the mitochondrial inner membrane. This longer isoform may help regulate energy metabolism in the mitochondria. A pseudogene of this gene is found on chromosome 9. Alternative splicing and the use of multiple translation start codons results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2015]
Gene Info
Gene Group
"C2 tensin-type domain containing|PTEN protein phosphatases|Phosphoinositide phosphatases"
Locus Type
gene with protein product
Location
10q23.31
Ensembl
ENSG00000171862
Associated Conditions (96)
Cowden syndrome 1
Hereditary cancer-predisposing syndrome
PTEN hamartoma tumor syndrome
Macrocephaly-autism syndrome
Familial meningioma
Glioma susceptibility 2
Familial prostate cancer
Breast and/or ovarian cancer
Prostate cancer
PTEN-related disorder
Diffuse pediatric-type high-grade glioma
H3-wildtype and IDH-wildtype
Melanoma
Vater association with macrocephaly and ventriculomegaly
Bannayan-Riley-Ruvalcaba syndrome
Cowden syndrome
Diffuse midline glioma
H3 K27M-mutant
Hereditary breast ovarian cancer syndrome
Neoplasm
+76 more conditions
Key Variants
RS1045014545
Conflicting classifications of pathogenicity
Cowden syndrome 1, Cowden syndrome 1
Health Risk
RS1050226735
Conflicting classifications of pathogenicity
Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
Health Risk
RS1057520525
Conflicting classifications of pathogenicity
Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome, Cowden syndrome 1
Health Risk
RS1057523132
Conflicting classifications of pathogenicity
Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome
Health Risk
RS1057523975
Conflicting classifications of pathogenicity
PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome, Cowden syndrome 1
Health Risk
RS1060500118
Conflicting classifications of pathogenicity
PTEN hamartoma tumor syndrome, Cowden syndrome 1, PTEN hamartoma tumor syndrome
Health Risk
RS1060500121
Conflicting classifications of pathogenicity
PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome, Glioma susceptibility 2
Health Risk
RS1060500125
Conflicting classifications of pathogenicity
PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome
Health Risk
RS1060500128
Conflicting classifications of pathogenicity
PTEN hamartoma tumor syndrome, PTEN hamartoma tumor syndrome
Health Risk
RS1060503839
Conflicting classifications of pathogenicity
PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome, Breast and/or ovarian cancer
Health Risk
RS1060503841
Conflicting classifications of pathogenicity
PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome, Cowden syndrome 1
Health Risk
RS1064794169
Conflicting classifications of pathogenicity
PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome
Health Risk
All Variants (1069)
RSID Category Clinical Significance Conditions
RS1057518425 Health Risk Likely pathogenic PTEN hamartoma tumor syndrome, Glioma susceptibility 2, Hereditary cancer-predisposing syndrome
RS1057519724 Health Risk Likely pathogenic PTEN hamartoma tumor syndrome, Neoplasm, PTEN hamartoma tumor syndrome
RS1057522285 Health Risk Likely pathogenic Neoplasm, Neoplasm
RS1060500124 Health Risk Likely pathogenic PTEN hamartoma tumor syndrome, Cowden syndrome 1, PTEN hamartoma tumor syndrome
RS1064792911 Health Risk Likely pathogenic PTEN hamartoma tumor syndrome, PTEN hamartoma tumor syndrome
RS1064793243 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome, Malignant tumor of breast
RS1064793325 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS1064793345 Health Risk Likely pathogenic Macrocephaly-autism syndrome, Cowden syndrome 1, PTEN hamartoma tumor syndrome
RS1064795967 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome
RS1064796128 Health Risk Likely pathogenic
RS1085308044 Health Risk Likely pathogenic PTEN hamartoma tumor syndrome, PTEN hamartoma tumor syndrome, PTEN hamartoma tumor syndrome
RS1085308046 Health Risk Likely pathogenic PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome, Cowden syndrome 1
RS1085308056 Health Risk Likely pathogenic PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome, Melanoma
RS1114167621 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, Cowden syndrome 1, PTEN hamartoma tumor syndrome
RS1114167624 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome, Cowden syndrome 1
RS1114167633 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS1114167648 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS1114167650 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, Cowden syndrome 1, PTEN hamartoma tumor syndrome
RS1114167656 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome, Autism
RS1114167664 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS1114167666 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS1114167667 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, Macrocephaly-autism syndrome, PTEN hamartoma tumor syndrome
RS1114167680 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome
RS1194768011 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome
RS121909223 Health Risk Likely pathogenic Cowden syndrome 1, PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome
RS121909225 Health Risk Likely pathogenic Cowden syndrome 1, PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome
RS121909237 Health Risk Likely pathogenic Squamous cell carcinoma of the head and neck, Cowden syndrome 1, Squamous cell carcinoma of the head and neck
RS121909238 Health Risk Likely pathogenic Macrocephaly-autism syndrome, PTEN hamartoma tumor syndrome, Cowden syndrome 1
RS121909240 Health Risk Likely pathogenic Macrocephaly-autism syndrome, PTEN hamartoma tumor syndrome, Macrocephaly-autism syndrome
RS121913291 Health Risk Likely pathogenic Cowden syndrome 1, PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome
RS121913294 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome, PTEN hamartoma tumor syndrome
RS1295420243 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS1303165645 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, Melanoma, Macrocephaly-autism syndrome
RS1313989099 Health Risk Likely pathogenic
RS138336847 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome, Intellectual disability
RS139767111 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome
RS1554825174 Health Risk Likely pathogenic Cowden syndrome 1, Cowden syndrome 1
RS1554825207 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS1554890324 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome, Cowden syndrome 1
RS1554890398 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome
RS1554893765 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome, Neurodevelopmental delay
RS1554897240 Health Risk Likely pathogenic PTEN hamartoma tumor syndrome, Cowden syndrome 1, Hereditary cancer-predisposing syndrome
RS1554897271 Health Risk Likely pathogenic Hereditary cancer, PTEN-related disorder, Hereditary cancer
RS1554897889 Health Risk Likely pathogenic Cowden syndrome 1, PTEN hamartoma tumor syndrome, Glioma susceptibility 2
RS1554898088 Health Risk Likely pathogenic Seizure, Hereditary cancer-predisposing syndrome, Seizure
RS1554898107 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS1554898113 Health Risk Likely pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS1554898138 Health Risk Likely pathogenic PTEN hamartoma tumor syndrome, Glioma susceptibility 2, Hereditary cancer-predisposing syndrome
RS1554898197 Health Risk Likely pathogenic PTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome, PTEN hamartoma tumor syndrome
RS1554898225 Health Risk Likely pathogenic
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