KIF23

kinesin family member 23
OMIM: 605064, Gene2Phenotype

4 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green KIF23 in Cytopenias and congenital anaemias Level 3: Anaemias and red cell disorders Level 2: Haematological disorders Version 1.118	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green UKGTN Phenotypes Enzyme Disorder Congenital dyserythropoietic anemia type III CDA III Congenital dyserythropoietic anemia (CDA)
Green KIF23 in Rare anaemia Version 3.8 Latest signed off version: v3.0 (22 Mar 2023)	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources North West GLH Yorkshire and North East GLH London South GLH NHS GMS Expert Review Green Wessex and West Midlands GLH Phenotypes Congenital dyserythropoietic anemia (CDA) Enzyme Disorder CDA III Anaemia, dyserythropoietic congenital, type III Congenital dyserythropoietic anemia type III 605064 Congenital dyserythropoietic anaemia type 3
Amber KIF23 in Cytopenia - NOT Fanconi anaemia Version 3.34 Latest signed off version: v3.0 (22 Mar 2023)	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Amber North West GLH NHS GMS Wessex and West Midlands GLH Phenotypes CDA III Congenital dyserythropoietic anemia (CDA) Congenital dyserythropoietic anemia type III Enzyme Disorder
Green KIF23 in Severe Paediatric Disorders Version 1.184	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Next Generation Children Project Expert Review Green Expert list Phenotypes neonatal anemia Congenital dyserythropoietic anemia type III