KIF23

kinesin family member 23
OMIM: 605064, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Amber KIF23 in Bone Marrow Failure


Level 2: Haematological disorders
Version 1.93

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Expert list
Phenotypes
  • Anaemia, congenital dyserythropoietic, type IIIA 105600

Red KIF23 in Hydrops fetalis


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.313

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Congenital dyserythropoietic anaemia

Amber KIF23 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Anaemia, congenital dyserythropoietic, type IIIA 105600

Amber KIF23 in Red cell disorders


Level 2: Haematological disorders
Version 1.24

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • Yorkshire and North East GLH
  • NHS GMS
  • Wessex and West Midlands GLH
  • North West GLH
  • London South GLH
  • Expert list
Phenotypes
  • Anaemia, congenital dyserythropoietic, type IIIA 105600