abnormal urine ph Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in urinary pH, indicating alterations in urine acidity or alkalinity (Mammalian Phenotype Ontology, MP_0009348)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009348
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Genes

20 gene mutations causing the abnormal urine ph phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTRAP angiotensin II receptor-associated protein
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
ATP6V1B1 ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1
CLCN5 chloride channel, voltage-sensitive 5
CLDN16 claudin 16
FOXI1 forkhead box I1
NOS1 nitric oxide synthase 1 (neuronal)
NOS2 nitric oxide synthase 2, inducible
OXGR1 oxoglutarate (alpha-ketoglutarate) receptor 1
RHCG Rh family, C glycoprotein
SLC12A7 solute carrier family 12 (potassium/chloride transporter), member 7
SLC16A10 solute carrier family 16 (aromatic amino acid transporter), member 10
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC26A7 solute carrier family 26 (anion exchanger), member 7
SLC2A9 solute carrier family 2 (facilitated glucose transporter), member 9
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4
TRPV5 transient receptor potential cation channel, subfamily V, member 5
UMOD uromodulin
UPK3A uroplakin 3A