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Protein Coding Gene : Egln2 egl-9 family hypoxia-inducible factor 2

Primary Identifier  MGI:1932287 Organism  mouse, laboratory
Chromosome  7 NCBI Gene Number  112406
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable ferrous iron binding activity; oxygen sensor activity; and peptidyl-proline 4-dioxygenase activity. Predicted to be involved in several processes, including cell redox homeostasis; cellular response to hypoxia; and peptidyl-proline hydroxylation to 4-hydroxy-L-proline. Predicted to be located in nucleoplasm. Predicted to be active in cytoplasm and nucleus. Is expressed in brain; cerebral cortex; hippocampus; and olfactory epithelium. Human ortholog(s) of this gene implicated in renal cell carcinoma. Orthologous to human EGLN2 (egl-9 family hypoxia inducible factor 2).
PHENOTYPE: Homozygotes are viable with no apparent abnormalities in cardiovascular, hematopoietic, or placental morphology and development. [provided by MGI curators]
  • synonyms:
  • 0610011A13Rik,
  • RIKEN cDNA 0610011A13 gene,
  • MGD-MRK-36364,
  • SM-20,
  • Hif-p4h-1,
  • MGI:107787,
  • Ier4,
  • egl-9 family hypoxia-inducible factor 2,
  • MGI:2142358,
  • MGI:1915611,
  • immediate early response 4,
  • Egln2,
  • Phd1

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