ANO6

anoctamin 6
OMIM: 608663, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green ANO6 in Bleeding and Platelet Disorders


Level 2: Haematological disorders
Version 1.43

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Scott syndrome, MIM# 262890
  • MONDO:0009885

Green ANO6 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Scott syndrome, MIM# 262890
  • MONDO:0009885

Green ANO6 in Transplant Co-Morbidity Superpanel


Level 2: Screening
Version 0.18

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • MONDO:0009885
  • Scott syndrome, MIM# 262890