PHLDA2 - pleckstrin homology like domain family A member 2 Gene
Also Known as IPL; BRW1C; BWR1C; HLDA2; TSSC3
Species: Homo sapiens
About PHLDA2
This gene has 1 transcript (splice variant), 1 gene allele, 172 orthologues and 2 paralogues. Biased expression in placenta (RPKM 44.3), colon (RPKM 8.6) and 3 other tissues.
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, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast Cancer. This gene has been shown to be imprinted, with preferential expression from the maternal allele in placenta and liver. [provided by RefSeq, Oct 2010]
PHLDA2 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_003311.4 | NP_003302.1 | pleckstrin homology-like domain family A member 2 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
32296183 | GOA |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
pleckstrin homology-like domain family A member 2 |
|
PHLDA2 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
PHLDA2 | Q53GA4 | FCHO1 | Homo sapiens | A0A0C3SFZ9 | 32296183 | |
|
Intra
|
PHLDA2 | Q53GA4 | FCHO1 | Homo sapiens | A0A0C3SFZ9 | 32296183 | |
|
Intra
|
PHLDA2 | Q53GA4 | SSX2 | Homo sapiens | Q16385-2 | 32296183 | |
|
Intra
|
PHLDA2 | Q53GA4 | SSX2 | Homo sapiens | Q16385-2 | 32296183 | |
|
Intra
|
PHLDA2 | Q53GA4 | OTUB2 | Homo sapiens | Q96DC9 | 32296183 | |
|
Intra
|
PHLDA2 | Q53GA4 | OTUB2 | Homo sapiens | Q96DC9 | 32296183 | |
|
Intra
|
PHLDA2 | Q53GA4 | OTUB2 | Homo sapiens | Q96DC9 | 32296183 |
Recombinant PHLDA2 Proteins
| Cat. No. | Product Name | Accession | Purity |
|---|---|---|---|
| HY-P71202 | PHLDA2 Protein, Human (His) | Q53GA4 (M1-P152) | ≥ 90%, as determined by reducing SDS-PAGE. |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Beckwith-Wiedemann Syndrome |
|
|
| Esophageal Adenoid Cystic Carcinoma |
|
|
| Hydatidiform Mole, Recurrent, 1 |
|
|
| Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies |
|
|
| Hellp Syndrome |
|
|
| Silver-Russell Syndrome 1 |
|
|
| Gestational Trophoblastic Neoplasm |
|
|
| Adult Syndrome |
|
|
| Breast Cancer |
|
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Bos taurus | PHLDA2 | VGNC | VGNC:32836 |
| Rattus norvegicus | PHLDA2 | RGD | RGD:1304755 |
| Mus musculus | PHLDA2 | MGD | MGI:1202307 |
| Felis catus | PHLDA2 | VGNC | VGNC:105832 |
| Others | PHLDA2 | NCBI |