RUNX1

runt related transcription factor 1
OMIM: 151385, Gene2Phenotype

8 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 8 panels
Green RUNX1 in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 1.52	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 1.114 Component of the following Super Panels: Immunological disorders_SuperPanel	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 1.2374	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 0.131	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Leukemia, acute myeloid, MIM# 601626
Green RUNX1 in Incidentalome_PREGEN_DRAFT Version 0.43	review	Unknown	Sources NSW Health Pathology Expert Review Green
Green RUNX1 in IBMDx study Version 0.35	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 BabyScreen+ newborn screening Level 2: Screening Version 1.116	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 Superpanel Level 2: Screening Version 0.18	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Green Phenotypes Platelet disorder, familial, with associated myeloid malignancy, MIM# 601399