| Gene Symbol | ZMYM3 |
| Entrez Gene ID | 9203 |
| Full Name | zinc finger MYM-type containing 3 |
| Synonyms | DXS6673E,MYM,XFIM,ZNF198L2,ZNF261 |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | This gene is located on the X chromosome and is subject to X inactivation. It is highly conserved in vertebrates and most abundantly expressed in the brain. The encoded protein is a component of histone deacetylase-containing multiprotein complexes that function through modifying chromatin structure to keep genes silent. A chromosomal translocation (X;13) involving this gene is associated with X-linked cognitive disability. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2010]. |
| Disorder MIM: |








































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