KIF2A, kinesin family member 2A, 3796

N. diseases: 81; N. variants: 29
Disease: Malformations of Cortical Development ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1955869
Disease: Malformations of Cortical Development
Malformations of Cortical Development 		0.310 Biomarker disease BEFREE Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical development. 29077851 2018
CUI: C1955869
Disease: Malformations of Cortical Development
Malformations of Cortical Development 		0.310 Biomarker disease CTD_human Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. 23603762 2013