JAK3

Janus kinase 3
OMIM: 600173, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green JAK3 in Mendeliome Version 1.3512	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes SCID, autosomal recessive, T-negative/B-positive type MIM# 600802 Tags treatable
Green JAK3 in Severe Combined Immunodeficiency Level 2: Immunological disorders Version 1.27 Component of the following Super Panels: Immunological disorders_SuperPanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Melbourne Genomics Health Alliance Immunology Flagship Victorian Clinical Genetics Services Phenotypes SCID, autosomal recessive, T-negative/B-positive type MIM# 600802 Tags treatable
Green JAK3 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 SCID, autosomal recessive, T-negative/B-positive type, 600802 (3)
Green JAK3 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category A gene Expert Review Green Phenotypes SCID, autosomal recessive, T-negative/B-positive type
Green JAK3 in Prepair 1000+ Level 2: Screening Version 2.14	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes SCID, autosomal recessive, T-negative/B-positive type, 600802 (3)
Green JAK3 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green BabySeq Category A gene BeginNGS Phenotypes SCID, autosomal recessive, T-negative/B-positive type, MIM#600802 Tags treatable immunological
Green JAK3 in Prepair 500+ Level 2: Screening Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Severe combined immunodeficiency, autosomal recessive, T-negative/B-positive type MIM#600802