RIPK1

receptor interacting serine/threonine kinase 1
OMIM: 603453, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

No list RIPK1 in Infantile enterocolitis & monogenic inflammatory bowel disease

Level 3: Gastrointestinal disorders
Level 2: Gastroenterological disorders
Version 1.24

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
Phenotypes
  • Immunodeficiency 57, MIM#618108

Green RIPK1 in COVID-19 research


Level 2: Viral research
Version 1.80

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Literature
  • London North GLH
  • NHS GMS
  • North West GLH
  • Expert Review Green
  • NHS GMS
  • North West GLH
  • London North GLH
  • Expert Review Green
  • Literature
Phenotypes
  • Severe immunodeficiency, arthritis, and intestinal inflammation
  • Immunodeficiency 57, 618108

Green RIPK1 in Primary immunodeficiency


Version 2.478
Latest signed off version: v2.1 (24 Feb 2020)

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • North West GLH
  • London North GLH
  • Expert Review Green
  • Literature
Phenotypes
  • Immunodeficiency 57, 618108
  • Severe immunodeficiency, arthritis, and intestinal inflammation
Tags
  • for-review

Green RIPK1 in Severe Paediatric Disorders


Version 1.84

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Next Generation Children Project
  • Expert Review Green
  • Expert list
Phenotypes
  • Immunodeficiency 57, 618108