TPTE2 (transmembrane phosphoinositide 3-phosphatase and tensin homolog 2)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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93492 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Transmembrane phosphoinositide 3-phosphatase and tensin homolog 2 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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TPTE2 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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TPIP |
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Chromosome
Chromosome number
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13 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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13q12.11 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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TPIP is a member of a large class of membrane-associated phosphatases with substrate specificity for the 3-position phosphate of inositol phospholipids.[supplied by OMIM, Jul 2002] |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | ||||||||||||||||
| UniProt ID | Q6XPS3 | |||||||||||||||
| Protein name | Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase TPTE2 (EC 3.1.3.67) (Lipid phosphatase TPIP) (TPTE and PTEN homologous inositol lipid phosphatase) | |||||||||||||||
| Protein function | Acts as a lipid phosphatase, removing the phosphate in the D3 position of the inositol ring from phosphatidylinositol 3,4,5-trisphosphate. ; [Isoform 4]: Shows no phosphoinositide phosphatase activity. {EC | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Isoform 3 is expressed in testis, brain and stomach while isoform 4 seems to be testis-specific. {ECO:0000269|PubMed:11716755}. | |||||||||||||||
| Sequence |
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| Sequence length | 522 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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