DNAH14

dynein axonemal heavy chain 14
OMIM: 603341, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Red DNAH14 in Respiratory ciliopathies including non-CF bronchiectasis


Level 2: Respiratory
Version 5.4
Latest signed off version: v5.3 (12 Aug 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • ClinGen
Phenotypes
  • primary ciliary dyskinesia, MONDO:0016575
Red DNAH14 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 8.7
Latest signed off version: v8.0 (12 Aug 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
Phenotypes
  • Neurodevelopmental disorder
Red DNAH14 in DDG2P


Version 8.2
Latest signed off version: v8.0 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • DD-Gene2Phenotype
    Phenotypes
    • DNAH14-related Neurodevelopmental disorder
    Red DNAH14 in Intellectual disability


    Level 2: Developmental disorders
    Version 11.31
    Latest signed off version: v11.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature