ZMYM3
Function
Plays a role in the regulation of cell morphology and cytoskeletal organization.
Involvement in disease
Intellectual developmental disorder, X-linked 112
XLID112
A neurodevelopmental disorder characterized by developmental delay, impaired intellectual development, language and motor delay, autism or autistic traits, and variable dysmorphic features.
None
The disease is caused by variants affecting the gene represented in this entry.
A chromosomal aberration involving ZMYM3 may be a cause of X-linked intellectual disability in Xq13.1. Translocation t(X;13)(q13.1;q31).
Tissue Specificity
Most abundant in brain, moderate in muscle and heart, low in other tissues except placenta.
Cellular localization
- Nucleus
Alternative names
DXS6673E, KIAA0385, ZNF261, ZMYM3, Zinc finger MYM-type protein 3, Zinc finger protein 261