1. Genes and Genomic Entities
  2. WDR63

WDR63

WD repeat domain 63
Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red WDR63 in Rare multisystem ciliopathy disorders

Level 3: Congenital malformations caused by ciliopathies
Level 2: Ciliopathies
Version 1.180

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Other
Phenotypes
  • occipital encephalocele and inconsistent brain lobulation
  • ciliopathy-like disorder
Tags
  • deletions
  • new-gene-name
Red WDR63 in Neurological ciliopathies


Level 2: Neurology
Version 6.13
Latest signed off version: v6.0 (30 Apr 2025)

Component of the following Super Panels:

  • Hereditary ataxia and cerebellar anomalies - childhood onset
  • Paediatric disorders
  • Rare multisystem ciliopathy Super panel

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    Phenotypes
    • occipital encephalocele and inconsistent brain lobulation
    • ciliopathy-like disorder
    Tags
    • new-gene-name