| Primary Identifier | MGI:1333812 | Organism | mouse, laboratory |
| Chromosome | 10 | NCBI Gene Number | 17192 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Enables DNA binding activity and chromatin binding activity. Acts upstream of or within in utero embryonic development; negative regulation of macromolecule biosynthetic process; and tissue development. Located in cytoplasm and nucleus. Part of NuRD complex and heterochromatin. Is expressed in several structures, including central nervous system; early conceptus; oocyte; and retina. Orthologous to human MBD3 (methyl-CpG binding domain protein 3). PHENOTYPE: Mice homozygous for disruptions in this gene experience deficiencies as embryos around implantation and die before birth. [provided by MGI curators] |
Features --> Cross References
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
