NAA25

N(alpha)-acetyltransferase 25, NatB auxiliary subunit
OMIM: 612755, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red NAA25 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 MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Literature
Phenotypes
  • craniosynostosis, MONDO:0015469