Basic Information

Symbol
ZMYM3
RNA class
mRNA
Alias
Zinc Finger MYM-Type Containing 3 DXS6673E Zinc Finger Protein 261 ZNF198L2 KIAA0385 ZNF261 MYM Zinc Finger MYM-Type Protein 3 Zinc Finger, Myeloproliferative, And Mental Retardation-Type 3 Zinc Finger, MYM-Type 3 XLID112 XFIM
Location (GRCh38)
Forensic tag(s)
Sudden cardiac death diagnosis

MANE select

Transcript ID
NM_201599.3
Sequence length
5536.0 nt
GC content
0.5466

Transcripts

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
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]

Forensic Context

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].