ARPC1B

actin related protein 2/3 complex subunit 1B
OMIM: 604223, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green ARPC1B in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 1.62	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia, MIM# 617718 Tags treatable
Green ARPC1B in Mendeliome Version 1.3512	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease 617718 Tags treatable
Green ARPC1B in Combined Immunodeficiency Level 2: Immunological disorders Version 1.138 Component of the following Super Panels: Immunological disorders_SuperPanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease 617718 Tags treatable
Green ARPC1B in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.110	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease, 617718 (3), Autosomal recessive
Green ARPC1B in Prepair 1000+ Level 2: Screening Version 2.14	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia MIM#617718
Green ARPC1B in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green BeginNGS Phenotypes Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia, MIM#617718 Tags treatable immunological
Green ARPC1B in Transplant Co-Morbidity Level 2: Screening Version 0.20	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Expert Review Green Phenotypes Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia, MIM# 617718