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Protein Coding Gene : Chd9 chromodomain helicase DNA binding protein 9

Primary Identifier  MGI:1924001 Organism  mouse, laboratory
Chromosome  8 NCBI Gene Number  109151
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 9.1.0)

Predicted to enable ATP binding activity and ATP hydrolysis activity. Acts upstream of or within chromatin organization. Predicted to be located in cytosol and nucleoplasm. Is expressed in bone; endochondral bone; and periosteum. Orthologous to human CHD9 (chromodomain helicase DNA binding protein 9).
PHENOTYPE: Mice homozygous for null mutations are viable and fertile, although growing oocytes exhibit a less loosened chromatin structure. [provided by MGI curators]
  • synonyms:
  • Chd9,
  • MGI:2444510,
  • AD013,
  • A330063D19Rik,
  • RIKEN cDNA A330063D19 gene,
  • 9030205D12Rik,
  • RIKEN cDNA 1810014J18 gene,
  • chromodomain helicase DNA binding protein 9,
  • 1810014J18Rik,
  • mKIAA0308,
  • RIKEN cDNA 9030205D12 gene,
  • MGI:1924942

Features --> Cross References

Genome

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0 CDSs

0 Exons

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0 Involved In Mutations

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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

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Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

7 Pathways

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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