Gene: KIF22 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		0.110 GeneticVariation disease BEFREE This condition has clinical overlap with autosomal dominantly inherited SEMD with joint laxity, leptodactylic type caused by recurrent missense variants in the kinesin family member 22 gene (KIF22). 26669664 2016
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		0.110 Biomarker disease HPO