KIF20A

kinesin family member 20A
OMIM: 605664, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red KIF20A in Paediatric or syndromic cardiomyopathy


Version 3.46
Latest signed off version: v3.0 (22 Mar 2023)

Component of the following Super Panels:

  • Unexplained death in infancy and sudden unexplained death in childhood
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • ?Cardiomyopathy, familial restrictive, 6, OMIM:619433