abnormal renal water reabsorbtion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the process by which water is passively transported out of the renal tubules back into the bloodstream (Mammalian Phenotype Ontology, MP_0010108)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010108
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6 gene mutations causing the abnormal renal water reabsorbtion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCY6 adenylate cyclase 6
AKR1B1 aldo-keto reductase family 1, member B1 (aldose reductase)
CLDN2 claudin 2
NOS1 nitric oxide synthase 1 (neuronal)
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC9A3 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3