PRICKLE3

prickle planar cell polarity protein 3
OMIM: 300111, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red PRICKLE3 in Leber hereditary optic neuropathy


Level 2: Mitochondrial
Version 2.10
Latest signed off version: v2.5 (22 Mar 2023)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Leber’s hereditary optic neuropathy
Red PRICKLE3 in Intellectual disability


Level 2: Developmental disorders
Version 9.285
Latest signed off version: v9.0 (30 Apr 2025)

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