Gene: KIF11 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3832
Gene Symbol: KIF11
KIF11 		0.100 CausalMutation phenotype CLINVAR Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations. 25124931 2014
Entrez Id: 3832
Gene Symbol: KIF11
KIF11 		0.100 CausalMutation phenotype CLINVAR Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: five novel mutations and review of the literature. 25115524 2014