PAX5

paired box 5
OMIM: 167414, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green PAX5 in Mendeliome Version 1.1902	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Neurodevelopmental disorder MONDO:0700092, PAX5-related Hypogammaglobulinaemia
Green PAX5 in Cancer Predisposition_Paediatric Level 2: Cancer Version 0.131	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes {Leukemia, acute lymphoblastic, susceptibility to, 3}, MIM# 615545
Amber PAX5 in Predominantly Antibody Deficiency Level 2: Immunological disorders Version 0.135 Component of the following Super Panels: Immunological disorders_SuperPanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Neurodevelopmental disorder MONDO:0700092, PAX5-related Hypogammaglobulinaemia
Green PAX5 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder MONDO:0700092, PAX5-related Hypogammaglobulinaemia
Red PAX5 in NCGC Version 0.2	review	Other	Sources NCGC Phenotypes Leukemia, acute lymphoblastic, susceptibility to, 3
Red PAX5 in TCGA_PANCAN_2018 Version 0.2	review	Other	Sources TCGA_PANCAN_2018 Phenotypes Leukemia, acute lymphoblastic, susceptibility to, 3
Red PAX5 in BabyScreen+ newborn screening Level 2: Screening Version 1.114	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Expert list Phenotypes {Leukemia, acute lymphoblastic, susceptibility to, 3} MIM#615545