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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
phosphatase and tensin homolog
Summary
- Gene Symbol
-
- PTEN
- Aliases
-
- MMAC1
- PTEN1
- TEP1
- mutated in multiple advanced cancers 1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative initiation
- Alternative splicing
- Apoptosis
- Autism spectrum disorder
- Cell projection
- Cytoplasm
- Disease variant
- Isopeptide bond
- Lipid metabolism
- Lipid-binding
- Neurogenesis
- Nucleus
- Phosphoprotein
- Protein phosphatase
- Reference proteome
- Secreted
- Synapse
- Tumor suppressor
- Ubl conjugation
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| regulation of protein stability | ||
| positive regulation of cell population proliferation | ||
| negative regulation of protein phosphorylation | ||
| negative regulation of keratinocyte migration | ||
| protein stabilization |
GO Hierarchy
- negative regulation of excitatory postsynaptic potential
biological process
metabolic process [inference]
cellular process [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of metabolic process [inference]
negative regulation of metabolic process [inference]
positive regulation of metabolic process [inference]
regulation of cellular metabolic process [inference]
negative regulation of cellular metabolic process [inference]
regulation of phosphorus metabolic process [inference]
negative regulation of phosphorus metabolic process [inference]
regulation of phosphate metabolic process [inference]
regulation of nitrogen compound metabolic process [inference]
regulation of macromolecule metabolic process [inference]
regulation of primary metabolic process [inference]
regulation of signaling [inference]
regulation of locomotion [inference]
positive regulation of biological process [inference]
negative regulation of biological process [inference]
negative regulation of metabolic process [inference]
negative regulation of cellular process [inference]
regulation of response to stimulus [inference]
regulation of developmental process [inference]
regulation of cellular process [inference]
regulation of cell communication [inference]
regulation of cellular metabolic process [inference]
negative regulation of cellular metabolic process [inference]
regulation of phosphorus metabolic process [inference]
negative regulation of phosphorus metabolic process [inference]
regulation of phosphate metabolic process [inference]
regulation of cell population proliferation [inference]
regulation of cell differentiation [inference]
negative regulation of cellular process [inference]
regulation of cellular component organization [inference]
regulation of cell cycle [inference]
regulation of molecular function [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| PML body | ||
| Schmidt-Lanterman incisure | ||
| extracellular region | ||
| cytoplasmic side of plasma membrane | ||
| neuron projection |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| PDZ domain binding | ||
| ubiquitin ligase activator activity | ||
| anaphase-promoting complex binding | ||
| protein serine/threonine phosphatase activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- phosphatase
- Functional Category
-
- E: Amino acid transport and metabolism
- P: Inorganic ion transport and metabolism
- T: Signal transduction mechanisms
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0014667 | disease of metabolism | |
| DOID:0050657 | Bannayan-Riley-Ruvalcaba syndrome | |
| DOID:0050696 | fetal alcohol spectrum disorder | |
| DOID:0050866 | oral squamous cell carcinoma | |
| DOID:0050933 | ovarian serous carcinoma | |
| DOID:0060041 | autism spectrum disorder | |
| DOID:0060669 | cerebral cavernous malformation | |
| DOID:0060867 | macrocephaly-autism syndrome | |
| DOID:0080072 | intestinal pseudo-obstruction | |
| DOID:0080191 | PTEN hamartoma tumor syndrome |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000034 | Hydrocele testis |
| HP:0000036 | Abnormal penis morphology |
| HP:0000040 | Long penis |
| HP:0000053 | Macroorchidism |
| HP:0000077 | Abnormality of the kidney |
| HP:0000098 | Tall stature |
| HP:0000105 | Enlarged kidney |
| HP:0000107 | Renal cyst |
| HP:0000130 | Abnormality of the uterus |
| Disease ID | Disease Name |
|---|---|
| OMIM:605309 |
|
| OMIM:176807 |
|
| ORPHA:65285 |
|
| ORPHA:210548 |
|
| OMIM:613028 |
|
| ORPHA:2969 |
|
| OMIM:607174 |
|
| ORPHA:109 |
|
| ORPHA:137608 |
|
| ORPHA:397596 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP000810
- Gene Name
- phosphatase and tensin homolog
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 19211 | MGI:109583 | MOUSE25368 | ||
| 43991 | FB:FBgn0026379 | |||
| 50557 | RGD:61995 | RATNO20306 | ||
| 176869 | WB:WBGene00000913 | |||
| 368415 | ZFIN:ZDB-GENE-030616-47 | |||
| 399142 | Xenbase:XB-GENE-491437 | |||
| 403832 | CANLF10667 | |||
| 466142 | 9598_0:002bec | PANTR01087 | ||
| 540786 | BOVIN21124 | |||
| 794088 | ZFIN:ZDB-GENE-030131-3776 |
