KIF15

kinesin family member 15
OMIM: 617569, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Red KIF15 in Anophthalmia_Microphthalmia_Coloboma


Level 2: Ophthalmological disorders
Version 1.45

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Braddock-Carey syndrome 2 - MIM#619981

Red KIF15 in Bleeding and Platelet Disorders


Level 2: Haematological disorders
Version 1.55

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Braddock-Carey syndrome 2 - MIM#619981

Red KIF15 in Mendeliome


Version 1.2512

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Braddock-Carey syndrome 2 - MIM#619981

Red KIF15 in Microcephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.303

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Braddock-Carey syndrome 2 - MIM#619981

Red KIF15 in Pierre Robin Sequence


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.49

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Braddock-Carey syndrome 2 - MIM#619981