RUNX1

runt related transcription factor 1
OMIM: 151385, Gene2Phenotype

10 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 10 panels
Green RUNX1 in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 1.43	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 1.93	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 1.1902	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
Red RUNX1 in NCGC Version 0.2	review	Other	Sources NCGC Phenotypes Familial platelet disorder with associated myeloid malignancy
Red RUNX1 in TCGA_PANCAN_2018 Version 0.2	review	Other	Sources TCGA_PANCAN_2018 Phenotypes Familial platelet disorder with associated myeloid malignancy
Green RUNX1 in Incidentalome_PREGEN_DRAFT Version 0.43	review	Unknown	Sources NSW Health Pathology Expert Review Green
Green RUNX1 in IBMDx study Version 0.25	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 1.114	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