Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9928
Gene Symbol: KIF14
KIF14 		0.600 Biomarker disease GENOMICS_ENGLAND Loss-of-function mutations in KIF14 cause severe microcephaly and kidney development defects in humans and zebrafish. 30388224 2019
Entrez Id: 9928
Gene Symbol: KIF14
KIF14 		0.600 GermlineCausalMutation disease ORPHANET Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype. 24128419 2014
Entrez Id: 9928
Gene Symbol: KIF14
KIF14 		0.600 Biomarker disease GENOMICS_ENGLAND Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype. 24128419 2014
Entrez Id: 9928
Gene Symbol: KIF14
KIF14 		0.600 CausalMutation disease CLINVAR
Entrez Id: 9928
Gene Symbol: KIF14
KIF14 		0.600 Biomarker disease GENOMICS_ENGLAND