Misplaced Pages

DDX39

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Protein-coding gene in the species Homo sapiens


DDX39A
Identifiers
AliasesDDX39A, BAT1, BAT1L, DDX39, DDXL, URH49, DEAD-box helicase 39A, DExD-box helicase 39A
External IDsMGI: 1915528; HomoloGene: 68487; GeneCards: DDX39A; OMA:DDX39A - orthologs
Gene location (Human)
Chromosome 19 (human)
Chr.Chromosome 19 (human)
Chromosome 19 (human)Genomic location for DDX39AGenomic location for DDX39A
Band19p13.12Start14,408,798 bp
End14,419,383 bp
Gene location (Mouse)
Chromosome 8 (mouse)
Chr.Chromosome 8 (mouse)
Chromosome 8 (mouse)Genomic location for DDX39AGenomic location for DDX39A
Band8|8 C2Start84,441,806 bp
End84,453,521 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • left testis

  • right testis

  • granulocyte

  • ventricular zone

  • spleen

  • lymph node

  • mucosa of transverse colon

  • appendix

  • ganglionic eminence

  • upper lobe of left lung
Top expressed in
  • primitive streak

  • Paneth cell

  • endothelial cell of lymphatic vessel

  • hair follicle

  • abdominal wall

  • otic placode

  • medullary collecting duct

  • migratory enteric neural crest cell

  • epiblast

  • condyle
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

10212

68278

Ensembl

ENSG00000123136

ENSMUSG00000005481

UniProt

O00148

Q8VDW0

RefSeq (mRNA)

NM_001204057
NM_005804
NM_138998

NM_197982
NM_001363116
NM_001363117

RefSeq (protein)

NP_005795

NP_932099
NP_001350045
NP_001350046

Location (UCSC)Chr 19: 14.41 – 14.42 MbChr 8: 84.44 – 84.45 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

ATP-dependent RNA helicase DDX39 is an enzyme that in humans is encoded by the DDX39 gene.

This gene encodes a member of the DEAD box protein family. These proteins are characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD) and are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of the DEAD box protein family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000123136Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000005481Ensembl, 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. Peelman LJ, Chardon P, Nunes M, Renard C, Geffrotin C, Vaiman M, Van Zeveren A, Coppieters W, van de Weghe A, Bouquet Y, et al. (Aug 1995). "The BAT1 gene in the MHC encodes an evolutionarily conserved putative nuclear RNA helicase of the DEAD family". Genomics. 26 (2): 210–8. doi:10.1016/0888-7543(95)80203-X. PMID 7601445.
  6. ^ "Entrez Gene: DDX39 DEAD (Asp-Glu-Ala-Asp) box polypeptide 39".

Further reading

External links

PDB gallery
  • 1t5i: Crystal structure of the C-terminal domain of UAP56 1t5i: Crystal structure of the C-terminal domain of UAP56
  • 1t6n: Crystal structure of the N-terminal domain of human UAP56 1t6n: Crystal structure of the N-terminal domain of human UAP56
  • 1xti: Structure of Wildtype human UAP56 1xti: Structure of Wildtype human UAP56
  • 1xtj: structure of human UAP56 in complex with ADP 1xtj: structure of human UAP56 in complex with ADP
  • 1xtk: structure of DECD to DEAD mutation of human UAP56 1xtk: structure of DECD to DEAD mutation of human UAP56


Stub icon

This article on a gene on human chromosome 19 is a stub. You can help Misplaced Pages by expanding it.

Categories: