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Protein Coding Gene : Ptges3 prostaglandin E synthase 3

Primary Identifier  MGI:1929282 Organism  mouse, laboratory
Chromosome  10 NCBI Gene Number  56351
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables DNA polymerase binding activity. Involved in telomerase holoenzyme complex assembly and telomere maintenance via telomerase. Acts upstream of or within several processes, including glycogen biosynthetic process; intracellular glucocorticoid receptor signaling pathway; and prostaglandin biosynthetic process. Predicted to be located in actin filament; neuronal cell body; and perinuclear region of cytoplasm. Predicted to be part of protein folding chaperone complex and telomerase holoenzyme complex. Predicted to be active in cytosol and nucleus. Is expressed in several structures, including liver and skin. Orthologous to human PTGES3 (prostaglandin E synthase 3).
PHENOTYPE: Disruption of gene function results in neonatal lethality, respiratory system abnormalities, as well as skin morphological and physiological defects. [provided by MGI curators]
  • synonyms:
  • sid3177,
  • RIKEN cDNA 5730442A20 gene,
  • cPGES,
  • telomerase binding protein, p23,
  • prostaglandin E synthase 3,
  • Ptges,
  • p23 cochaperone,
  • 5730442A20Rik,
  • Tebp,
  • Ptges3,
  • MGI:1913886

Features --> Cross References

Genome

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

19 Pathways

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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