PHLDA1

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

Pleckstrin homology-like domain family A member 1 (PHLDA1) is a protein that in humans is encoded by the PHLDA1 gene.[5][6][7]

AliasesPHLDA1, DT1P1B11, PHRIP, TDAG51, pleckstrin homology like domain family A member 1
End76,031,776 bp[1]
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PHLDA1
Identifiers
AliasesPHLDA1, DT1P1B11, PHRIP, TDAG51, pleckstrin homology like domain family A member 1
External IDsOMIM: 605335; MGI: 1096880; HomoloGene: 7203; GeneCards: PHLDA1; OMA:PHLDA1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_007350

NM_009344

RefSeq (protein)

NP_031376

NP_033370

Location (UCSC)Chr 12: 76.03 – 76.03 MbChr 10: 111.34 – 111.34 Mb
PubMed search[3][4]
Wikidata
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This gene encodes an evolutionarily conserved proline-histidine rich nuclear protein. The encoded protein may play an important role in the anti-apoptotic effects of insulin-like growth factor-1.[7]

Interactions

PHLDA1 has been shown to interact with RPL14,[8] EIF3D[8] and PABPC4.[8]

References

Further reading

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