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Protein Coding Gene : Hspa12a heat shock protein 12A
Primary Identifier  MGI:1920692 Organism  mouse, laboratory
Chromosome  19 NCBI Gene Number  73442
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable ATP binding activity. Predicted to be located in cytoplasm and nucleus. Is expressed in nervous system; retina; and white fat. Orthologous to human HSPA12A (heat shock protein family A (Hsp70) member 12A).
PHENOTYPE: Homozygous knockout affects glucose metabolism, reducing susceptibility to diet-induced obesity. It also reduces diet-induced damage to the liver through suppression of macrophage recruitment, increases LPS-induced liver damage and increases susceptibility to ischemic brain injury. [provided by MGI curators]
  • synonyms:
  • MGI:2147750,
  • Hspa12a,
  • Gm19925,
  • MGI:2147692,
  • mKIAA0417,
  • MGI:2147603,
  • heat shock protein 12A,
  • predicted gene, 19925,
  • AW556406,
  • expressed sequence AW556406,
  • expressed sequence AI840429,
  • RIKEN cDNA 1700063D12 gene,
  • AW048913,
  • MGI:5012110,
  • AI840429,
  • expressed sequence AW048913,
  • 1700063D12Rik
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