RIPK1

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

4 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
No list RIPK1 in Infantile enterocolitis & monogenic inflammatory bowel disease Level 3: Gastrointestinal disorders Level 2: Gastroenterological disorders Version 1.45	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Phenotypes Immunodeficiency 57, OMIM:618108
Green RIPK1 in COVID-19 research Level 2: Viral research Version 1.147	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 or monogenic inflammatory bowel disease Level 2: Immunology Version 9.9 Latest signed off version: v9.0 (6 May 2026)	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources NHS GMS North West GLH London North GLH Expert Review Green Literature Phenotypes Autoinflammation with episodic fever and lymphadenopathy, OMIM:618852 Immunodeficiency 57 with autoinflammation, OMIM: 618108
Green RIPK1 in Autoinflammatory disorders Level 2: Immunology Version 3.7 Latest signed off version: v3.0 (6 May 2026)	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green NHS GMS Research Literature Expert Review Expert list Phenotypes Autoinflammation with episodic fever and lymphadenopathy, OMIM:618852 Immunodeficiency 57 with autoinflammation, OMIM: 618108