CORO1A

coronin 1A
OMIM: 605000, Gene2Phenotype

3 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Green CORO1A in COVID-19 research Level 2: Viral research Version 1.146	review	BIALLELIC, autosomal or pseudoautosomal	Sources IUIS Classification February 2018 London North GLH GOSH PID v.8.0 NHS GMS GRID V2.0 Victorian Clinical Genetics Services North West GLH ESID Registry 20171117 Combined B and T cell defect v1.12 Expert Review Green NHS GMS North West GLH London North GLH IUIS Classification February 2018 Victorian Clinical Genetics Services Expert Review Green ESID Registry 20171117 GRID V2.0 GOSH PID v.8.0 Combined B and T cell defect v1.12 Phenotypes Combined immunodeficiency Immunodeficiency 8 hypogammaglobulinaemia, combined immunodeficiency Coronin-1A deficiency Atypical Severe Combined Immunodeficiency (Atypical SCID) Detectable thymus, EBV Immunodeficiencies affecting cellular and humoral immunity Omenn syndrome Severe combined immunodeficiency (SCID)
Amber CORO1A in Epidermodysplasia verruciformis Level 2: Dermatology Version 1.7 Latest signed off version: v1.3 (15 Oct 2020)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber
Green CORO1A in Primary immunodeficiency or monogenic inflammatory bowel disease Level 2: Immunology Version 8.78 Latest signed off version: v8.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Other NHS GMS North West GLH London North GLH IUIS Classification February 2018 Victorian Clinical Genetics Services ESID Registry 20171117 GRID V2.0 GOSH PID v.8.0 Combined B and T cell defect v1.12 Phenotypes Immunodeficiency 8 Combined immunodeficiency hypogammaglobulinaemia, combined immunodeficiency Coronin-1A deficiency Atypical Severe Combined Immunodeficiency (Atypical SCID) Severe combined immunodeficiency (SCID) Omenn syndrome Detectable thymus, EBV Immunodeficiencies affecting cellular and humoral immunity