PRICKLE3

prickle planar cell polarity protein 3
OMIM: 300111, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red PRICKLE3 in Intellectual disability


Level 2: Developmental disorders
Version 10.16
Latest signed off version: v10.0 (6 May 2026)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
    Sources
    • Expert Review Red