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Protein Coding Gene : Pgm1 phosphoglucomutase 1
Primary Identifier  MGI:97565 Organism  mouse, laboratory
Chromosome  4 NCBI Gene Number  72157
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables phosphoglucomutase activity. Acts upstream of or within glucose metabolic process. Predicted to be located in Z disc. Predicted to be active in cytosol. Is expressed in cerebral cortex; embryo; heart; and liver. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation It; endometrial cancer; and teratoma. Orthologous to human PGM1 (phosphoglucomutase 1).
PHENOTYPE: Homozygous knockout is embryonic lethal, while heterozygous KO leads to reduced viability. [provided by MGI curators]
  • synonyms:
  • RIKEN cDNA 2610020G18 gene,
  • MGI:6194611,
  • phosphoglucomutase 1,
  • AI098105,
  • MGI:2140187,
  • AA407108,
  • MGD-MRK-13276,
  • Pgm2,
  • phosphoglucomutase 2,
  • Pgm1,
  • MGI:2140115,
  • Pgm1a,
  • Pgm-2,
  • MGD-MRK-13279,
  • MGI:6194613,
  • 2610020G18Rik,
  • MGI:1919407,
  • phosphoglucomutase 1a,
  • expressed sequence AI098105,
  • expressed sequence AA407108
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