GLIS2, GLIS family zinc finger 2, 84662

N. diseases: 67; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.310 GeneticVariation group BEFREE Glis2/NPHP7 is a transcriptional regulator mutated in type 7 nephronophthisis, an autosomal recessive ciliopathy associated with cystic and fibrotic kidney disease as well as characteristic extrarenal manifestations. 26083374 2015
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.310 Biomarker group CTD_human Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis. 17618285 2007