KIF26B, kinesin family member 26B, 55083

N. diseases: 38; N. variants: 6
Disease: Papillorenal syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1852759
Disease: Papillorenal syndrome
Papillorenal syndrome 		0.010 GeneticVariation disease BEFREE The results of this study identify several new mutations of PAX2, and sequence variants in four additional genes, including a novel potentially pathogenic mutation in KIF26B, which may play a role in the pathogenesis of RCS. 26571382 2015