RUNX1:Ensemblv90

runt related transcription factor 1
OMIM: 151385, ClinGen, DECIPHER

18 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 18 panels
Green RUNX1 in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 1.63	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 1.131 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 1.3802	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
Red RUNX1 in NCGC Version 0.3	0 reviews	Other	Sources NCGC Phenotypes Familial platelet disorder with associated myeloid malignancy
Red RUNX1 in TCGA_PANCAN_2018 Version 0.3	0 reviews	Other	Sources TCGA_PANCAN_2018 Phenotypes Familial platelet disorder with associated myeloid malignancy
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 1.141	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
Green RUNX1 in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Green Phenotypes Platelet disorder, familial, with associated myeloid malignancy, MIM# 601399
Green RUNX1 in Bone Marrow Failure Level 2: Haematological disorders Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Expert Review Green Phenotypes Platelet disorder, familial, with associated myeloid malignancy, MIM# 601399
Green RUNX1 in Cancer Predisposition_Paediatric Level 2: Cancer Version 1.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Expert Review Green Phenotypes Leukemia, acute myeloid, MIM# 601626
Green RUNX1 in Additional findings_Adult Level 2: Screening Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Green Phenotypes Platelet disorder, familial, with associated myeloid malignancy, MIM# 601399
Green RUNX1 in IBMDx study Version 1.0	1 review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green IBMDx Study Expert Review Green Phenotypes Platelet disorder, familial, with associated myeloid malignancy, MIM# 601399
Green RUNX1 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 2.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources ClinGen Expert Review Green 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 1.0	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Platelet disorder, familial, with associated myeloid malignancy, MIM# 601399