abnormal renal water homeostasis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the kidney processes involved in the maintenance of an internal steady state of water in the body (Mammalian Phenotype Ontology, MP_0011444)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011444
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Genes

9 gene mutations causing the abnormal renal water homeostasis 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)
AQP1 aquaporin 1 (Colton blood group)
AQP3 aquaporin 3 (Gill blood group)
AQP4 aquaporin 4
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