C21orf59

chromosome 21 open reading frame 59
OMIM: 615494, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green C21orf59 in Ciliary Dyskinesia


Level 2: Respiratory disorders
Version 1.47

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 26, MIM# 615500
Tags
  • founder
  • new gene name

Green C21orf59 in Heterotaxy


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.36

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 26, MIM# 615500
Tags
  • founder
  • new gene name

Green C21orf59 in Mendeliome


Version 1.2374

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 26, MIM# 615500
Tags
  • founder
  • new gene name

Green C21orf59 in Fetal anomalies


Version 1.314

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genomics England PanelApp
  • Victorian Clinical Genetics Services
Phenotypes
  • Primary ciliary dyskinesia 26, MONDO:0014211
  • Ciliary dyskinesia, primary, 26, OMIM:615500
Tags
  • founder
  • new gene name