Genetic loci influencing kidney function and chronic kidney disease.
Data(s) |
2010
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Resumo |
Using genome-wide association, we identify common variants at 2p12-p13, 6q26, 17q23 and 19q13 associated with serum creatinine, a marker of kidney function (P = 10(-10) to 10(-15)). Of these, rs10206899 (near NAT8, 2p12-p13) and rs4805834 (near SLC7A9, 19q13) were also associated with chronic kidney disease (P = 5.0 x 10(-5) and P = 3.6 x 10(-4), respectively). Our findings provide insight into metabolic, solute and drug-transport pathways underlying susceptibility to chronic kidney disease. |
Identificador |
http://serval.unil.ch/?id=serval:BIB_55509FC8B9C3 isbn:1546-1718[electronic], 1061-4036[linking] pmid:20383145 doi:10.1038/ng.566 isiid:000277179500005 |
Idioma(s) |
en |
Direitos |
info:eu-repo/semantics/openAccess |
Fonte |
Nature Genetics, vol. 42, no. 5, pp. 373-375 |
Palavras-Chave | #Biological Transport; Creatinine/blood; Cystatin C/metabolism; Type="Geographic">Europe; Gene Expression Regulation; Genetic Markers/genetics; Genetic Predisposition to Disease; Genetic Variation; Genome-Wide Association Study; Genotype; Glomerular Filtration Rate; Humans; Kidney/physiology; Kidney Failure, Chronic/genetics; Kidney Failure, Chronic/pathology; Models, Genetic ; Colaus Study |
Tipo |
info:eu-repo/semantics/article article |