PHLDA2

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PHLDA2
Identifiers
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
View/Edit HumanView/Edit Mouse

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

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

  1. ^ a b c ENSG00000274538 GRCh38: Ensembl release 89: ENSG00000181649, ENSG00000274538Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000010760Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. PMID 9328465
    .
  6. .
  7. ^ a b "Entrez Gene: PHLDA2 pleckstrin homology-like domain, family A, member 2".

Further reading

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