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Gene : DHX9 Homo sapiens

Name  ? DExH-box helicase 9 Cytological Location  1q25.3
Brief Description  DExH-box helicase 9
Description  This gene encodes a member of the DEAH-containing family of RNA helicases. The encoded protein is an enzyme that catalyzes the ATP-dependent unwinding of double-stranded RNA and DNA-RNA complexes. This protein localizes to both the nucleus and the cytoplasm and functions as a transcriptional regulator. This protein may also be involved in the expression and nuclear export of retroviral RNAs. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 11 and 13.[provided by RefSeq, Feb 2010]
  • synonyms:
  • NDH2,
  • NDH II,
  • LKP,
  • DDX9,
  • DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 9,
  • RHA,
  • DHX9,
  • DEAH (Asp-Glu-Ala-His) box helicase 9,
  • NDHII,
  • nuclear DNA helicase II,
  • uc001gpr.4,
  • leukophysin,
  • OTTHUMG00000035337,
  • RNA helicase A,
  • DDX9,
  • RHA,
  • LKP,
  • HGNC:2750,
  • NM_030588,
  • L13848
  • identifiers:
  • 1660,
  • ENSG00000135829,
  • DHX9

Genome feature

Region: gene ? Length: 48636  
Location: 1:182839347-182887982 Cyto location: 1q25.3

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0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene Ontology

Gene --> GO terms.



11 SN Ps

5 Cross References

16 Data Sets

5 Homologues

3 Located Features

97 Rna Seq Results