KIF17

kinesin family member 17
OMIM: 605037, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red KIF17 in Structural eye disease


Level 2: Ophthalmology
Version 4.37
Latest signed off version: v4.0 (7 Aug 2024)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Microphthalmia, MONDO:0021129
  • Coloboma, MONDO:0001476