PHLDA2 (pleckstrin homology like domain family A member 2)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 7262 |
| Gene name | Pleckstrin homology like domain family A member 2 |
| Gene symbol | PHLDA2 |
| Synonyms (NCBI Gene) |
BRW1CBWR1CHLDA2IPLTSSC3
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| Chromosome | 11 |
| Chromosome location | 11p15.4 |
| Summary | This gene is located in a cluster of imprinted genes on chromosome 11p15.5, which is considered to be an important tumor suppressor gene region. Alterations in this region may be associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarco |
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miRNA
miRNA information provided by mirtarbase database.
100
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q53GA4 | |
| Protein name | Pleckstrin homology-like domain family A member 2 (Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene C protein) (Imprinted in placenta and liver protein) (Tumor-suppressing STF cDNA 3 protein) (Tumor-suppressing subchromosomal transferable f | |
| Protein function | Plays a role in regulating placenta growth. May act via its PH domain that competes with other PH domain-containing proteins, thereby preventing their binding to membrane lipids (By similarity). | |
| Family and domains | ||
| Tissue specificity | TISSUE SPECIFICITY: Expressed in placenta and adult prostate gland. In placenta, it is present in all cells of the villous cytotrophoblast. The protein is absent in cells from hydatidiform moles. Hydatidiform mole is a gestation characterized by abnormal | |
| Sequence |
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| Sequence length | 152 | |
| Interactions | View interactions | |