DHX29

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

DExH-box helicase 29 (DHX29) is a 155 kDa protein that in humans is encoded by the DHX29 gene.[5]

AliasesDHX29, DDX29, DEAH-box helicase 29, DExH-box helicase 29
End55,307,694 bp[1]
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DHX29
Identifiers
AliasesDHX29, DDX29, DEAH-box helicase 29, DExH-box helicase 29
External IDsOMIM: 612720; MGI: 2145374; HomoloGene: 10387; GeneCards: DHX29; OMA:DHX29 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_019030
NM_001345964
NM_001345965

NM_172594

RefSeq (protein)

NP_001332893
NP_001332894
NP_061903

NP_766182

Location (UCSC)Chr 5: 55.26 – 55.31 MbChr 13: 113.06 – 113.11 Mb
PubMed search[3][4]
Wikidata
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Function

This gene encodes a member of the DEAH (Asp-Glu-Ala-His) subfamily of proteins, part of the DEAD (Asp-Glu-Ala-Asp) box family of RNA helicases. The encoded protein functions in translation initiation, and is specifically required for ribosomal scanning across stable mRNA secondary structures during initiation codon selection.[6] This protein may also play a role in sensing virally derived cytosolic nucleic acids.[7] Knockdown of this gene results in reduced protein translation and impaired proliferation of cancer cells.[8]

Interactions

See also

References

Further reading

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