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Protein Coding Gene : Cept1 choline/ethanolaminephosphotransferase 1
Primary Identifier  MGI:2139793 Organism  mouse, laboratory
Chromosome  3 NCBI Gene Number  99712
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables phosphotransferase activity, for other substituted phosphate groups. Acts upstream of or within phosphatidylcholine biosynthetic process. Located in endoplasmic reticulum membrane. Is expressed in alimentary system; cranium; nervous system; nose; and urinary system. Orthologous to human CEPT1 (choline/ethanolamine phosphotransferase 1).
PHENOTYPE: Conditional homozygous knockout in skeletal muscle leads to improved glucose tolerance, increased insulin sensitivity and muscle weakness in mice fed a high fat diet. [provided by MGI curators]
  • synonyms:
  • expressed sequence AI788721,
  • 9930118K05Rik,
  • AI788721,
  • expressed sequence BB118941,
  • choline/ethanolaminephosphotransferase 1,
  • RIKEN cDNA 9930118K05 gene,
  • MGI:2140023,
  • Cept1,
  • BB118941
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2 Involved In Mutations

Trail: ProteinCodingGene

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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.

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6 Pathways

Trail: ProteinCodingGene

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

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