Targeted gene(s)/phenotype under study

RBM10 (OMIM 300080)


Loss of function variants in RBM10 are well known to cause TARP-syndrome, a severe X-linked recessive syndrome with malformations, global developmental delay, and early death of affected males. Missense variants in the RBM10-gene have so far not been proven to be pathogenic. We have collected a cohort of families with RBM10-variants – missense variants, splice variants and loss of function variants – and we are conducting a PhD study of the genotype-phenotype correlation and supporting functional studies.

We welcome further cases of rare variants in the RBM10-gene – all types of variants are included.

Coordinating clinician/researcher

Christina Fagerberg


Department of Clinical Genetics
Odense University Hospital
Odense, Denmark

Specific requirements beyond clinical data and genotype data sharing

  • Re-analysis of DNA samples : No
  • Resampling of patients : Yes
  • Linked to a translational/basic research project? Yes