KIF6

kinesin family member 6
OMIM: 613919, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red KIF6 in Mendeliome


Version 2.543

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Infertility disorder, MONDO:0005047, KIF6-related
  • Neurodevelopmental disorder, MONDO:0700092, KIF6-related

Red KIF6 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.135

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, KIF6-related

Red KIF6 in Infertility and Recurrent Pregnancy Loss


Version 2.41

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Infertility disorder, MONDO:0005047, KIF6-related