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Protein Coding Gene : Pcgf3 polycomb group ring finger 3

Primary Identifier  MGI:1916837 Organism  mouse, laboratory
Chromosome  5 NCBI Gene Number  69587
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables histone H2AK119 ubiquitin ligase activity. Involved in random inactivation of X chromosome. Part of PcG protein complex. Colocalizes with X chromosome. Is expressed in several structures, including branchial arch; central nervous system; limb; otocyst; and urinary system. Orthologous to human PCGF3 (polycomb group ring finger 3).
PHENOTYPE: Mice homozygous for a transgenic gene disruption exhibit limb defects and spleen agenesis. [provided by MGI curators]
  • synonyms:
  • polycomb group ring finger 3,
  • expressed sequence AI662857,
  • Pcgf3,
  • AI662857,
  • DONG1,
  • ring finger protein 3,
  • 2310035N15Rik,
  • RNF3A,
  • Rnf3,
  • D630042K08Rik,
  • RIKEN cDNA D630042K08 gene,
  • RIKEN cDNA 2310035N15 gene,
  • MGI:2445213,
  • MGI:2140956

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

2 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

 

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0 Driver For