PALB2

partner and localizer of BRCA2
OMIM: 610355, Gene2Phenotype

18 panels

Panel Reviews Mode of inheritance Details
18 panels

Green PALB2 in Bone Marrow Failure


Level 2: Haematological disorders
Version 1.114

Component of the following Super Panels:

  • Immunological disorders_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 Chromosome Breakage Disorders


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.21

    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 0.314

    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 1.15

    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 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 1.314

    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 0.35

    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 1.116

    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

    Green PALB2 in Wilms Tumour


    Level 2: Cancer Predisposition
    Version 1.0

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    • Expert list
    Phenotypes
    • Wilms tumor, MONDO:0006058
    • Fanconi anemia complementation group N, MONDO:0012565
    • Fanconi anemia, complementation group N, MIM#610832

    Green PALB2 in Pancreatic Cancer


    Level 2: Cancer Predisposition
    Version 1.1

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert Review
    • Expert list
    Phenotypes
    • Malignant pancreatic neoplasm, MONDO:0009831
    • PALB2-related cancer predisposition, MONDO:0700272
    • Breast-ovarian cancer, familial, susceptibility to, 5, MIM#620442
    • Pancreatic cancer, susceptibility to, 3, MIM#613348

    Green PALB2 in Prostate Cancer


    Level 2: Cancer Predisposition
    Version 1.1

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert Review
    • Expert list
    Phenotypes
    • Prostate cancer, MONDO:0008315
    • PALB2-related cancer predisposition, MONDO:0700272
    • Breast-ovarian cancer, familial, susceptibility to, 5, MIM#620442
    • Pancreatic cancer, susceptibility to, 3, MIM#613348

    Green PALB2 in Ovarian Cancer


    Level 2: Cancer Predisposition
    Version 1.1

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert Review
    • Expert list
    Phenotypes
    • Ovarian cancer, MONDO:0008170
    • PALB2-related cancer predisposition, MONDO:0700272
    • Breast-ovarian cancer, familial, susceptibility to, 5, MIM#620442
    • Pancreatic cancer, susceptibility to, 3, MIM#613348

    Green PALB2 in Breast Cancer


    Level 2: Cancer Predisposition
    Version 1.1

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert Review
    • Expert list
    Phenotypes
    • Breast cancer, MONDO:0007254
    • PALB2-related cancer predisposition, MONDO:0700272
    • Breast-ovarian cancer, familial, susceptibility to, 5, MIM#620442
    • Pancreatic cancer, susceptibility to, 3, MIM#613348