FAS

Fas cell surface death receptor
OMIM: 134637, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green FAS in Mendeliome


Version 2.0

2 reviews BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • autoimmune lymphoproliferative syndrome MONDO:0017979

Green FAS in Disorders of immune dysregulation


Level 2: Immunological disorders
Version 2.0

2 reviews Unknown
Sources
  • Expert Review Green
  • Melbourne Genomics Health Alliance Immunology Flagship
  • Victorian Clinical Genetics Services
  • Expert Review Green
  • Victorian Clinical Genetics Services

Red FAS in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 2.0

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • BeginNGS
Phenotypes
  • Autoimmune lymphoproliferative syndrome, type IA, MIM# 601859

Green FAS in Autoimmune Lymphoproliferative Syndrome


Level 2: Immunological disorders
Version 2.0

1 review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Autoimmune lymphoproliferative syndrome, type IA MIM#601859