abnormal renal transport Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly of the directed movement of substances through the kidney (Mammalian Phenotype Ontology, MP_0011417)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011417
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Genes

20 gene mutations causing the abnormal renal 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
ATP6V1B1 ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1
CLCN5 chloride channel, voltage-sensitive 5
CLDN2 claudin 2
CYP4A11 cytochrome P450, family 4, subfamily A, polypeptide 11
NOS1 nitric oxide synthase 1 (neuronal)
NPPA natriuretic peptide A
NR3C2 nuclear receptor subfamily 3, group C, member 2
SGK1 serum/glucocorticoid regulated kinase 1
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
SLC14A2 solute carrier family 14 (urea transporter), member 2
SLC6A18 solute carrier family 6 (neutral amino acid transporter), member 18
SLC6A19 solute carrier family 6 (neutral amino acid transporter), member 19
SLC9A3 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3
TMEM27 transmembrane protein 27