PHLDA2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Pleckstrin homology-like domain family A member 2 is a protein that in humans is encoded by the PHLDA2 gene.[5][6][7]

AliasesPHLDA2, BRW1C, BWR1C, HLDA2, IPL, TSSC3, pleckstrin homology like domain family A member 2
End2,929,420 bp[1]
Quick facts Identifiers, Aliases ...
PHLDA2
Identifiers
AliasesPHLDA2, BRW1C, BWR1C, HLDA2, IPL, TSSC3, pleckstrin homology like domain family A member 2
External IDsOMIM: 602131; MGI: 1202307; HomoloGene: 2482; GeneCards: PHLDA2; OMA:PHLDA2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_003311

NM_009434

RefSeq (protein)

NP_003302

NP_033460

Location (UCSC)Chr 11: 2.93 – 2.93 MbChr 7: 143.06 – 143.06 Mb
PubMed search[3][4]
Wikidata
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This gene is one of several genes in the imprinted gene domain of 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. Studies of the mouse gene, however, which is also located in an imprinted gene domain, have shown that the product of this gene regulates placental growth.[7]

References

Further reading

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