abnormal urine chloride ion level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any change in the amount of chloride ion in the urine (Mammalian Phenotype Ontology, MP_0011458)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011458
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Genes

16 gene mutations causing the abnormal urine chloride ion level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAMTS1 ADAM metallopeptidase with thrombospondin type 1 motif, 1
ADCY6 adenylate cyclase 6
AKR1B1 aldo-keto reductase family 1, member B1 (aldose reductase)
CLDN4 claudin 4
CLDN7 claudin 7
KCNK5 potassium channel, two pore domain subfamily K, member 5
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
SLC4A11 solute carrier family 4, sodium borate transporter, member 11
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2
SPP1 secreted phosphoprotein 1
STK39 serine threonine kinase 39
TFCP2L1 transcription factor CP2-like 1
TGFB1 transforming growth factor, beta 1
UMOD uromodulin
UPK2 uroplakin 2
WNK4 WNK lysine deficient protein kinase 4