Kidney adysplasia and variable hydronephrosis, a new mutation affecting the odd - Skipped related 1 gene in the mouse, causes variable defects in kidney development and hydronephrosis

M T Davisson, S a Cook, E C Akeson, D Liu, C Heffner, P Gudis, H Fairfield, S a Murray
American Journal of Physiology - Renal Physiology2015
Many genes, including odd-skipped related 1 (Osr1), are involved in regulation of mammalian kidney development. We describe here a new recessive mutation (kidney adysplasia and variable hydronephrosis, kavh) in the mouse that leads to downregulation of Osr1 transcript, causing several kidney defects: agenesis, hypoplasia, and hydronephrosis with variable age of onset. The mutation is closely associated with a reciprocal translocation, T(12;17)4Rk, whose Chromosome 12 breakpoint is upstream from Osr1. The kavh/kavh mutant provides a model to study kidney development and test therapies for hydronephrosis.
Share

Want to see more papers in your research area? 

Get a customized bibliography.

Request Now

Publication Right Sidebar