TICRR

TOPBP1 interacting checkpoint and replication regulator
OMIM: 613298, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red TICRR in Rare syndromic craniosynostosis or isolated multisuture synostosis

Level 3: Craniosynostosis syndromes
Level 2: Skeletal disorders
Version 5.1
Latest signed off version: v5.0 (1 May 2024)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review
Phenotypes
  • coronal craniosynostosis, cardiomyopathy