TTC25

tetratricopeptide repeat domain 25
OMIM: 617095, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green TTC25 in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 0.418

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • primary ciliary dyskinesia 35 MONDO:0014910
Tags
  • new gene name

Green TTC25 in Ciliary Dyskinesia


Level 2: Respiratory disorders
Version 1.39

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
Phenotypes
  • Ciliary dyskinesia, primary, 35 (MIM#617092)
Tags
  • new gene name

Green TTC25 in Heterotaxy


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.32

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 35 (MIM#617092)
Tags
  • new gene name

Green TTC25 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 35 (MIM#617092)
Tags
  • new gene name

Green TTC25 in Fetal anomalies


Version 1.255

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genomics England PanelApp
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 35 (MIM#617092)
Tags
  • new gene name