| 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] |