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Protein Coding Gene : Kdm7a lysine (K)-specific demethylase 7A

Primary Identifier  MGI:2443388 Organism  mouse, laboratory
Chromosome  6 NCBI Gene Number  338523
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables histone H3K27me2/H3K27me3 demethylase activity and histone H3K9 demethylase activity. Involved in positive regulation of DNA-templated transcription. Predicted to be located in nucleolus and nucleoplasm. Human ortholog(s) of this gene implicated in melanoma. Orthologous to human KDM7A (lysine demethylase 7A).
PHENOTYPE: Homozygous mutants exhibit abnormal hair follicle, tail, sebaceous gland, rib, and vertebrae morphology and decreased circulating iron levels. [provided by MGI curators]
  • synonyms:
  • expressed sequence BB041802,
  • BB041802,
  • Kdm7a,
  • predicted gene, ENSMUSG00000073143,
  • lysine (K)-specific demethylase 7A,
  • A630082K20Rik,
  • RIKEN cDNA A630082K20 gene,
  • MGI:2141725,
  • jumonji C domain-containing histone demethylase 1 homolog D (S. cerevisiae),
  • mKIAA1718,
  • ENSMUSG00000073143,
  • MGI:3642369,
  • Jhdm1d

Features --> Cross References

Genome

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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

3 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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