PRICKLE3

prickle planar cell polarity protein 3
OMIM: 300111, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red PRICKLE3 in Mendeliome


Version 1.1902

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
  • Literature
Phenotypes
  • Leber’s hereditary optic neuropathy MIM#535000