TTC12

tetratricopeptide repeat domain 12
OMIM: 610732, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
No list TTC12 in Primary ciliary disorders

Level 3: Respiratory ciliopathies
Level 2: Ciliopathies
Version 1.42

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
Phenotypes
  • Ciliary dyskinesia
Amber TTC12 in Respiratory ciliopathies including non-CF bronchiectasis


Version 3.10
Latest signed off version: v3.0 (22 Mar 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert list
Phenotypes
  • Ciliary dyskinesia, primary, 45, OMIM:618801
  • MONDO:0032924
Tags
  • watchlist
Red TTC12 in DDG2P


Version 3.90
Latest signed off version: v3.1 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • DD-Gene2Phenotype
    Phenotypes
    • TTC12-related Primary Ciliary Dyskinesia