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Protein Coding Gene : Ddx39b DEAD box helicase 39b

Primary Identifier  MGI:99240 Organism  mouse, laboratory
Chromosome  17 NCBI Gene Number  53817
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable several functions, including ATP hydrolysis activity; ATP-dependent protein binding activity; and RNA binding activity. Predicted to be involved in several processes, including RNA metabolic process; positive regulation of cell growth involved in cardiac muscle cell development; and positive regulation of macromolecule biosynthetic process. Located in nuclear speck. Is expressed in embryo. Human ortholog(s) of this gene implicated in type 1 diabetes mellitus. Orthologous to human DDX39B (DExD-box helicase 39B).
PHENOTYPE: Mice homozygous for a null allele exhibit complete preweaning lethality while mice heterozygous for the allele exhibit increased susceptibility to gamma radiation. [provided by MGI curators]
  • synonyms:
  • D17H6S81E,
  • 0610030D10Rik,
  • DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B,
  • MGD-MRK-16027,
  • DNA segment, Chr 17, human D6S81E,
  • Bat1,
  • MGD-MRK-1499,
  • Bat1a,
  • expressed sequence AI428441,
  • DEAD box helicase 39b,
  • MGD-MRK-7732,
  • RIKEN cDNA 0610030D10 gene,
  • MGD-MRK-1506,
  • MGI:3035179,
  • Bat-1,
  • D6S81Eh,
  • HLA-B-associated transcript 1,
  • MGC:19235,
  • HLA-B-associated transcript 1A,
  • Ddx39b,
  • AI428441,
  • MGC:38799,
  • MGI:1915639,
  • DNA segment, Chr 17, human D6S81E 1,
  • D17H6S81E-1,
  • MGD-MRK-15997

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1 Involved In Mutations

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