abnormal renal protein reabsorption Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the process in which proteins are taken up from the collecting ducts and proximal and distal loops of the nephron (Mammalian Phenotype Ontology, MP_0011445)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011445
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2 gene mutations causing the abnormal renal protein reabsorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CLCN5 chloride channel, voltage-sensitive 5
SLC15A2 solute carrier family 15 (oligopeptide transporter), member 2