PanelApp
  1. Genes and Genomic Entities
  2. RUNX1

RUNX1

runt related transcription factor 1
OMIM: 151385, Gene2Phenotype

9 panels

Panel Reviews Mode of inheritance Details
9 panels

Green RUNX1 in Bleeding and Platelet Disorders


Level 2: Haematological disorders
Version 1.62

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Platelet disorder, familial, with associated myeloid malignancy, MIM# 601399

Green RUNX1 in Bone Marrow Failure


Level 2: Haematological disorders
Version 1.129

Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Platelet disorder, familial, with associated myeloid malignancy, MIM# 601399

    Green RUNX1 in Mendeliome


    Version 1.3512

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Platelet disorder, familial, with associated myeloid malignancy, MIM# 601399
    • Leukemia, acute myeloid, MIM# 601626

    Green RUNX1 in Cancer Predisposition_Paediatric


    Level 2: Cancer
    Version 0.132

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Leukemia, acute myeloid, MIM# 601626

    Green RUNX1 in Additional findings_Adult


    Level 2: Screening
    Version 1.130

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Platelet disorder, familial, with associated myeloid malignancy, MIM# 601399

    Green RUNX1 in Incidentalome_PREGEN_DRAFT


    Version 0.43

    		0 reviews Unknown
    Sources
    • NSW Health Pathology
    • Expert Review Green

    Green RUNX1 in IBMDx study


    Version 0.38

    		1 review Unknown
    Sources
    • Expert Review Green
    • IBMDx Study
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Platelet disorder, familial, with associated myeloid malignancy, MIM# 601399

    Green RUNX1 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.140

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • ClinGen
    Phenotypes
    • Platelet disorder, familial, with associated myeloid malignancy, MIM# 601399
    Tags
    • for review
    • treatable
    • haematological

    Green RUNX1 in Transplant Co-Morbidity


    Level 2: Screening
    Version 0.20

    		0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert list
    • Expert Review Green
    Phenotypes
    • Platelet disorder, familial, with associated myeloid malignancy, MIM# 601399