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Protein Coding Gene : Poglut2 protein O-glucosyltransferase 2

Primary Identifier  MGI:1919300 Organism  mouse, laboratory
Chromosome  1 NCBI Gene Number  72050
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable UDP-glucosyltransferase activity and UDP-xylosyltransferase activity. Predicted to be involved in protein O-linked glycosylation via serine. Located in endoplasmic reticulum lumen. Is expressed in several structures, including brain; genitourinary system; gut; liver; and spleen. Orthologous to human POGLUT2 (protein O-glucosyltransferase 2).
PHENOTYPE: Homozygous null mice are viable, fertile, and present at expected ratios. [provided by MGI curators]
  • synonyms:
  • KDEL containing protein 1,
  • protein O-glucosyltransferase 2,
  • Kdelc1,
  • KDEL (Lys-Asp-Glu-Leu) containing 1,
  • MGI:1917775,
  • 5730416C13Rik,
  • 1810049A15Rik,
  • MGI:6285830,
  • RIKEN cDNA 5730416C13 gene,
  • Kdel1,
  • EP58,
  • RIKEN cDNA 1810049A15 gene,
  • Poglut2

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

1 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

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

0 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For