abnormal renal water transport Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the directed movement of water (H2O) by the kidney (Mammalian Phenotype Ontology, MP_0011443)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011443
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Genes

9 gene mutations causing the abnormal renal water transport 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