TRA2B-associated neurodevelopmental delay

Targeted gene(s)/phenotype under study :

  • Gene: TRA2B (OMIM *602719) 

Abstract :

TRA2B codes for Transformer-2 protein homolog beta, a factor putatively involved in the control of pre-mRNA splicing. Via international collaborative efforts we are aware of at least 7 index cases carrying different de novo TRA2B variants. All individuals have a developmental delay with variable additional clinical features including seizures, microcephaly, and growth retardation.

We would like to expand the cohort of patients with TRA2B variants in order to delineate the phenotype of this rare disease and are currently planning functional validation of pathogenicity of the variants

Coordinating clinicians /researchers: 

  • Tobias Haack

Institution :

University hospital Tübingen,

Tübingen, Germany

Contact : 

Specific requirements beyond clinical data and genotype data sharing:

  • Re-analysis of DNA samples : Yes
  • Resampling of patients : Yes
  • Linked to a translational/basic research project? Yes