FNIP1

folliculin interacting protein 1
OMIM: 610594, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green FNIP1 in Primary immunodeficiency or monogenic inflammatory bowel disease


Version 5.3
Latest signed off version: v5.0 (1 May 2024)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Primary Immunodeficiency
  • Agammaglobulinemia
  • Hypertrophic Cardiomyopathy
  • Neutropenia
Amber FNIP1 in Paediatric or syndromic cardiomyopathy


Version 4.3
Latest signed off version: v4.0 (1 May 2024)

Component of the following Super Panels:

  • Unexplained death in infancy and sudden unexplained death in childhood
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Hypertrophic Cardiomyopathy
    • Primary Immunodeficiency
    • Agammaglobulinemia
    • Neutropenia