KIF17

kinesin family member 17
OMIM: 605037, Gene2Phenotype

1 panel

Panel	Reviews	Mode of inheritance	Details
Red KIF17 in Structural eye disease Version 3.77 Latest signed off version: v3.0 (22 Mar 2023)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Microphthalmia, MONDO:0021129 Coloboma, MONDO:0001476

Panel

Reviews

Mode of inheritance

Details

Version 3.77
Latest signed off version: v3.0 (22 Mar 2023)

review

BIALLELIC, autosomal or pseudoautosomal