abnormal urine calcium level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any change in the amount of calcium in the urine (Mammalian Phenotype Ontology, MP_0002985)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002985
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Genes

26 gene mutations causing the abnormal urine calcium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AKR1B1 aldo-keto reductase family 1, member B1 (aldose reductase)
ATP6V1B1 ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B1
CASR calcium-sensing receptor
CAV1 caveolin 1, caveolae protein, 22kDa
CLCN5 chloride channel, voltage-sensitive 5
CLDN16 claudin 16
CLDN2 claudin 2
CLDN4 claudin 4
CRH corticotropin releasing hormone
CYP24A1 cytochrome P450, family 24, subfamily A, polypeptide 1
GCM2 glial cells missing homolog 2 (Drosophila)
GPRC6A G protein-coupled receptor, class C, group 6, member A
HNF1A HNF1 homeobox A
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
SLC26A1 solute carrier family 26 (anion exchanger), member 1
SLC34A1 solute carrier family 34 (type II sodium/phosphate cotransporter), member 1
SLC34A2 solute carrier family 34 (type II sodium/phosphate cotransporter), member 2
SLC34A3 solute carrier family 34 (type II sodium/phosphate cotransporter), member 3
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4
STK39 serine threonine kinase 39
TFAP2B transcription factor AP-2 beta (activating enhancer binding protein 2 beta)
TRPV5 transient receptor potential cation channel, subfamily V, member 5
UMOD uromodulin
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor