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
RS2493717435 Health Risk Pathogenic Cowden syndrome 1, PTEN hamartoma tumor syndrome, Cowden syndrome 1
RS2493717460 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493717485 Health Risk Pathogenic Gastric cancer, Gastric cancer
RS2493717607 Health Risk Pathogenic
RS2493717648 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493717941 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493717973 Health Risk Pathogenic Cowden syndrome 1, Prostate cancer, hereditary
RS2493718038 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493718057 Health Risk Pathogenic PTEN hamartoma tumor syndrome, Prostate cancer, hereditary
RS2493718073 Health Risk Pathogenic PTEN hamartoma tumor syndrome, PTEN hamartoma tumor syndrome
RS2493718152 Health Risk Pathogenic Glioma susceptibility 2, Glioma susceptibility 2
RS2493718158 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493718257 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493718282 Health Risk Pathogenic PTEN hamartoma tumor syndrome, PTEN hamartoma tumor syndrome
RS2493718556 Health Risk Pathogenic Macrocephaly-autism syndrome, Macrocephaly-autism syndrome
RS2493718697 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493718744 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493718775 Health Risk Pathogenic PTEN hamartoma tumor syndrome, PTEN hamartoma tumor syndrome
RS2493718807 Health Risk Pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS2493718859 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493718905 Health Risk Pathogenic Prostate cancer, hereditary, 1
RS2493718917 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493719108 Health Risk Pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS2493719115 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493719154 Health Risk Pathogenic Bannayan-Riley-Ruvalcaba syndrome, Bannayan-Riley-Ruvalcaba syndrome
RS2493719217 Health Risk Pathogenic PTEN hamartoma tumor syndrome, PTEN hamartoma tumor syndrome
RS2493719222 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493719243 Health Risk Pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS2493719289 Health Risk Pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS2493752971 Health Risk Pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS2493753029 Health Risk Pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS2493753054 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493753150 Health Risk Pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS2493753192 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493753199 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493753280 Health Risk Pathogenic Cowden syndrome, Cowden syndrome 1, PTEN hamartoma tumor syndrome
RS2493753371 Health Risk Pathogenic PTEN hamartoma tumor syndrome, PTEN hamartoma tumor syndrome
RS2493753426 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493753433 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493753571 Health Risk Pathogenic PTEN hamartoma tumor syndrome, PTEN hamartoma tumor syndrome
RS2493753593 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1, Cowden syndrome 1
RS2493753703 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493753707 Health Risk Pathogenic PTEN hamartoma tumor syndrome, PTEN hamartoma tumor syndrome
RS2493753765 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493753791 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493753839 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493753870 Health Risk Pathogenic Cowden syndrome 1, Cowden syndrome 1
RS2493753909 Health Risk Pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS2493754032 Health Risk Pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS2493754060 Health Risk Pathogenic Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
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