FOXJ1

forkhead box J1
OMIM: 602291, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green FOXJ1 in Ciliary Dyskinesia


Level 2: Respiratory disorders
Version 1.39

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Ciliary dyskinesia, primary, 43, MIM# 618699
  • hydrocephalus
  • chronic destructive airway disease
  • randomization of left/right body asymmetry

Green FOXJ1 in Heterotaxy


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.32

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Ciliary dyskinesia, primary, 43, MIM#618699
  • Hydrocephalus
  • chronic destructive airway disease
  • randomization of left/right body asymmetry

Green FOXJ1 in Hydrocephalus_Ventriculomegaly


Level 2: Neurology and neurodevelopmental disorders
Version 0.123

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Congenital hydrocephalus
  • Ciliary dyskinesia, primary, 43, MIM#618699

Green FOXJ1 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 43, MIM#618699
  • hydrocephalus
  • chronic destructive airway disease
  • randomization of left/right body asymmetry

Green FOXJ1 in Fetal anomalies


Version 1.255

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
  • Expert list
Phenotypes
  • Ciliary dyskinesia, primary, 43 - MIM# 618699