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Protein Coding Gene : Rere arginine glutamic acid dipeptide (RE) repeats

Primary Identifier  MGI:2683486 Organism  mouse, laboratory
Chromosome  4 NCBI Gene Number  68703
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Enables transcription coactivator activity and transcription corepressor activity. Acts upstream of or within chromatin remodeling; nervous system development; and positive regulation of DNA-templated transcription. Located in nucleus. Part of histone deacetylase complex. Is expressed in several structures, including alimentary system; eye; genitourinary system; nervous system; and vibrissa. Orthologous to human RERE (arginine-glutamic acid dipeptide repeats).
PHENOTYPE: Mice homozygous for disruptions in this gene display embryonic lethality with abnormalities in neural tube development, somite development, and in the embryonic heart. Mice homozygous for an ENU-induced allele exhibit narrow snouts, decreased body weight, renal agenesis and small eyes. [provided by MGI curators]
  • synonyms:
  • expressed sequence AI414665,
  • RIKEN cDNA 1110033A15 gene,
  • Atr2,
  • 1110033A15Rik,
  • MGI:2140608,
  • atrophin-2,
  • expressed sequence AW742570,
  • eyes 3,
  • MGI:3577417,
  • eye<m03Jus>,
  • mKIAA0458,
  • AW742570,
  • MGI:1915953,
  • eyes3,
  • AI414665,
  • arginine glutamic acid dipeptide (RE) repeats,
  • eye03,
  • Rere,
  • MGI:2140258

Features --> Cross References

Genome

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0 Canonical

0 CDSs

0 Exons

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1 Involved In Mutations

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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

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

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Disease

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Literature

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0 Driver For