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Protein Coding Gene : Gatad1 GATA zinc finger domain containing 1

Primary Identifier  MGI:1914460 Organism  mouse, laboratory
Chromosome  5 NCBI Gene Number  67210
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable sequence-specific DNA binding activity and zinc ion binding activity. Predicted to be involved in chromatin remodeling. Predicted to be located in nucleoplasm. Predicted to be active in nucleus. Is expressed in several structures, including eye; gonad; hemolymphoid system gland; liver; and lung. Human ortholog(s) of this gene implicated in dilated cardiomyopathy 2B. Orthologous to human GATAD1 (GATA zinc finger domain containing 1).
  • synonyms:
  • RIKEN cDNA 9130430G15 gene,
  • ENSMUSG00000073241,
  • RIKEN cDNA B330017N08 gene,
  • MGI:1916878,
  • MGI:1918759,
  • ocular development associated gene,
  • RIKEN cDNA 2310031E19 gene,
  • 2810047M21Rik,
  • GATA zinc finger domain containing 1,
  • RIKEN cDNA 2810047M21 gene,
  • Gatad1,
  • MGI:1924747,
  • predicted gene, ENSMUSG00000073241,
  • MGI:3711962,
  • 9130430G15Rik,
  • 8430439A17Rik,
  • RIKEN cDNA 8430439A17 gene,
  • 2310031E19Rik,
  • Odag,
  • B330017N08Rik

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

0 Involved In Mutations

0 Strain

0 Transcripts

1 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