KLF1

Kruppel like factor 1
OMIM: 600599, Gene2Phenotype

8 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 8 panels
Green KLF1 in Bone Marrow Failure Level 2: Haematological disorders Version 1.114 Component of the following Super Panels: Immunological disorders_SuperPanel	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Dyserythropoietic anaemia, congenital, type IVa, MIM# 613673 MONDO:0013355 Anaemia, congenital dyserythropoietic, type IVb, MIM#620969
Green KLF1 in Hydrops fetalis Level 2: Dysmorphic and congenital abnormality syndromes Version 0.324	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Congenital Dyserythropoietic Anemia Type IV, MIM#613673 Anaemia, congenital dyserythropoietic, type IVb, MIM#620969
Green KLF1 in Mendeliome Version 1.2374	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Dyserythropoietic anaemia, congenital, type IV, MIM# 613673 MONDO:0013355 Anaemia, congenital dyserythropoietic, type IVb, MIM#620969
Green KLF1 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green BabySeq Category C gene Phenotypes Dyserythropoietic anaemia, congenital, type IV, MIM# 613673 MONDO:0013355
Green KLF1 in Red cell disorders Level 2: Haematological disorders Version 1.29	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Yorkshire and North East GLH NHS GMS Wessex and West Midlands GLH North West GLH London South GLH Victorian Clinical Genetics Services Phenotypes Dyserythropoietic anaemia, congenital, type IV, MIM# 613673 MONDO:0013355 Anaemia, congenital dyserythropoietic, type IVb, MIM#620969
Green KLF1 in Fetal anomalies Version 1.314	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Phenotypes Dyserythropoietic anaemia, congenital, type IV MIM#613673 Anaemia, congenital dyserythropoietic, type IVb, MIM#620969
Green KLF1 in IBMDx study Version 0.35	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green IBMDx Study Victorian Clinical Genetics Services Phenotypes Dyserythropoietic anaemia, congenital, type IV, MIM# 613673 MONDO:0013355 Anaemia, congenital dyserythropoietic, type IVb, MIM#620969
Red KLF1 in BabyScreen+ newborn screening Level 2: Screening Version 1.116	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category C gene Phenotypes Dyserythropoietic anaemia, congenital, type IV, MIM# 613673