NQO1, NAD(P)H quinone dehydrogenase 1, 1728

N. diseases: 368; N. variants: 8
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0220726
Disease: Diastrophic dysplasia
Diastrophic dysplasia
0.030 GeneticVariation disease BEFREE Pendrin is closely related to a family of sulfate transport proteins that includes the rat sulfate-anion transporter (encoded by Sat-1; 29% amino acid sequence identity), the human diastrophic dysplasia sulfate transporter (encoded by DTD; 32%) and the human sulfate transporter 'downregulated in adenoma' (encoded by DRA; 45%). 10192399 1999
CUI: C0220726
Disease: Diastrophic dysplasia
Diastrophic dysplasia
0.030 Biomarker disease BEFREE Five fetuses in families with a previous history of DTD were studied by typing them and their relevant family members for DNA markers closely linked to the DTD gene. 8487268 1993
CUI: C0220726
Disease: Diastrophic dysplasia
Diastrophic dysplasia
0.030 GeneticVariation disease BEFREE Using these methods, we report striking linkage disequilibrium for diastrophic dysplasia (DTD) in Finland indicating that the DTD gene should lie within 0.06 centimorgans (or about 60 kilobases) of the CSF1R gene. 1345170 1992