PALB2

partner and localizer of BRCA2
OMIM: 610355, Gene2Phenotype

18 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 18 panels
Green PALB2 in Bone Marrow Failure Level 2: Haematological disorders Version 1.93	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Fanconi anaemia, complementation group N, MIM# 610832
Green PALB2 in Chromosome Breakage Disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 1.19	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Fanconi anaemia, complementation group N, MIM# 610832
Green PALB2 in Incidentalome Version 0.301	review	Unknown	Sources Expert Review Green Expert list Victorian Clinical Genetics Services Expert Review Green
Green PALB2 in Cancer Predisposition_Paediatric Level 2: Cancer Version 0.131	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green PALB2 in Radial Ray Abnormalities Level 2: Dysmorphic and congenital abnormality syndromes Version 1.10 Component of the following Super Panels: Limb and Digital Malformations SuperPanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Fanconi anaemia, complementation group N, MIM# 610832
Green PALB2 in Additional findings_Adult Level 2: Screening Version 0.166	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes {Breast cancer, susceptibility to} 114480
Green PALB2 in Homologous_recombination_deficiency_WTS_UMCCR Level 2: Cancer Version 0.43	review	Unknown	Sources Expert list Expert Review Green Tags umccr
Green PALB2 in Wilms Tumour Predisposition Level 2: Cancer predisposition Version 0.39	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Red PALB2 in CGC_86 Version 0.2	review	Other	Sources CGC_86 Phenotypes Fanconi anemia, complementation group N
Red PALB2 in NCGC Version 0.2	review	Other	Sources NCGC Phenotypes Fanconi anemia, complementation group N
Red PALB2 in TCGA_PANCAN_2018 Version 0.2	review	Other	Sources TCGA_PANCAN_2018 Phenotypes Fanconi anemia, complementation group N
Green PALB2 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green BabySeq Category C gene Phenotypes Fanconi anemia, complementation group N, MIM# 610832
Green PALB2 in Incidentalome_PREGEN_DRAFT Version 0.43	review	Unknown	Sources NSW Health Pathology Expert Review Green
Green PALB2 in Growth failure Version 1.76	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Victorian Clinical Genetics Services Phenotypes Fanconi anaemia, complementation group N, MIM# 610832
Green PALB2 in Fetal anomalies Version 1.255	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Fanconi anaemia, complementation group N, MIM# 610832
Green PALB2 in IBMDx study Version 0.25	review	Unknown	Sources Expert Review Green IBMDx Study Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Fanconi anaemia, complementation group N, MIM# 610832
Green PALB2 in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green BabySeq Category C gene Phenotypes Fanconi anemia, complementation group N, MIM# 610832 Tags treatable haematological
Green PALB2 in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Green Phenotypes {Breast cancer, susceptibility to} 114480