Resources
Want to learn more?
A new diagnosis can be overwhelming. Because ZMYND11 is so rare, there isn’t a lot of information out there for individuals and families. We’re working to bring the research and resources together here, in one place.
Our partners
Working together toward treatments
We partner with organizations that share our goal of faster answers and better care for families affected by rare neurological conditions.
Research partner
Unravel Biosciences
Unravel uses AI and patient data to find new uses for existing, FDA-approved drugs. Together, we’re running a drug repurposing screen for ZMYND11-related disorder.
Visit UnravelResearch consortium
COMBINEDBrain
COMBINEDBrain brings patient groups, researchers, clinicians and industry together to speed up research and treatments for rare neurological disorders.
Visit COMBINEDBrainPatient advocacy
DEEP
Developmental Epileptic Encephalopathies Patient Advocacy connects families, clinicians and researchers through education, caregiver support, research and advocacy.
Visit DEEPFamily education conference
Catch up on the talks
If you weren’t able to join our most recent family education conference, you can watch every talk below.
Join the ZMYND11 patient registry
We encourage everyone with ZMYND11 to join our patient registry with COMBINEDBrain.
Research library
Current research
Because ZMYND11 is so rare, information can be hard to find. We’re gathering the published research in one place.
Research papers
- ZMYND11-related syndromic intellectual disability: 16 patients delineating and expanding the phenotypic spectrum Yates et al. · via University of Sheffield
- ZMYND11 functions in bimodal regulation of latent genes and brain-like splicing to safeguard corticogenesis bioRxiv (not yet peer reviewed)
- Transgenic mice overexpressing mutant TDP-43 show aberrant splicing of neurological disorders-associated gene Zmynd11 prior to onset of motor symptoms Narayanan et al.
- ZMYND11 links histone H3.3K36me3 to transcription elongation and tumour suppression Wen et al.
Gene & protein databases
Our goal
To find treatments that improve the function of the ZMYND11 protein and reduce the severity of symptoms caused by the disorder.
When you have a rare disease, you face two battles: one, the illness itself, and the other, living in a world where so few people know what you are up against.
#raredisease
Every dollar counts when you’re finding a treatment.
Your gift helps fund research toward treatments for children and families living with ZMYND11-related disorder.