| ID | Sequence | Length | GC content |
|---|---|---|---|
| CAGACAAGGACAGAAAGGGGGCUGGAGGAGAAAGAGAGAGAGAGAUACA… | 6136 nt | 0.5486 | |
| AUUGAGGGGGGCGGACGCCGAGGGGGUGAACACGAGUGGGAAGCUAAGA… | 1930 nt | 0.5596 | |
| AUUGAGGGGGGCGGACGCCGAGGGGGUGAACACGAGUGGGAAGCUAAGA… | 5611 nt | 0.5457 | |
| AAAGGGGCCGCGACCCCUGUCCCGGCUGCUAGGGAGGGAGGUAGAGAAG… | 5536 nt | 0.5466 |
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]
A study in rhesus macaques identified the ZMYM3 as a differentially expressed gene downregulated in left ventricular tissue from animals with hypertrophic cardiomyopathy compared to healthy controls [Rivas et al. DOI:10.1038/s41598-024-82770-4].