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Protein Coding Gene : Egln3 egl-9 family hypoxia-inducible factor 3

Primary Identifier  MGI:1932288 Organism  mouse, laboratory
Chromosome  12 NCBI Gene Number  112407
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables peptidyl-proline dioxygenase activity. Involved in regulation of cell population proliferation and regulation of neuron apoptotic process. Acts upstream of or within cellular response to leukemia inhibitory factor. Predicted to be located in cytosol. Predicted to be active in cytoplasm and nucleus. Is expressed in several structures, including cardiovascular system; genitourinary system; gut; musculoskeletal system; and somite. Human ortholog(s) of this gene implicated in renal cell carcinoma. Orthologous to human EGLN3 (egl-9 family hypoxia inducible factor 3).
PHENOTYPE: Homozygous null mice display decreased apoptosis in SCG neurons, reduced adrenal medullary secretory capacity, abnormal adrenal medulla morphology, reduced circulating adrenaline and noradrenaline levels, and reduced systolic blood pressure. [provided by MGI curators]
  • synonyms:
  • Phd3,
  • egl-9 family hypoxia-inducible factor 3,
  • MGI:2144852,
  • expressed sequence AI505553,
  • AI648162,
  • 2610021G09Rik,
  • AI505553,
  • MGI:1919408,
  • MGI:2144873,
  • Egln3,
  • SM-20,
  • Hif-p4h-3,
  • RIKEN cDNA 2610021G09 gene,
  • expressed sequence AI648162

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0 CDSs

0 Exons

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1 Involved In Mutations

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

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Canonical gene --> Transcripts in specific strains.

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Mouse features --> Functions (GO terms)

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4 Pathways

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