increased circulating calcium level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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36 gene mutations causing the increased circulating 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)
B9D1 B9 protein domain 1
BAZ1B bromodomain adjacent to zinc finger domain, 1B
CASR calcium-sensing receptor
CLEC2D C-type lectin domain family 2, member D
COL4A5 collagen, type IV, alpha 5
CRH corticotropin releasing hormone
CYP24A1 cytochrome P450, family 24, subfamily A, polypeptide 1
DFNB31 deafness, autosomal recessive 31
FGF23 fibroblast growth factor 23
GALNT3 polypeptide N-acetylgalactosaminyltransferase 3
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
GRHL3 grainyhead-like 3 (Drosophila)
GSE1 Gse1 coiled-coil protein
HBP1 HMG-box transcription factor 1
HSPA4L heat shock 70kDa protein 4-like
JAK1 Janus kinase 1
KL klotho
LIX1L Lix1 homolog (chicken) like
MEN1 multiple endocrine neoplasia I
MPZL3 myelin protein zero-like 3
MRAP2 melanocortin 2 receptor accessory protein 2
MYO7A myosin VIIA
NDFIP2 Nedd4 family interacting protein 2
PTH1R parathyroid hormone 1 receptor
RXFP2 relaxin/insulin-like family peptide receptor 2
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC25A4 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4
SLC26A1 solute carrier family 26 (anion exchanger), member 1
SLC34A1 solute carrier family 34 (type II sodium/phosphate cotransporter), member 1
SLC34A3 solute carrier family 34 (type II sodium/phosphate cotransporter), member 3
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4
TM9SF4 transmembrane 9 superfamily protein member 4
UMOD uromodulin
WDR37 WD repeat domain 37
XDH xanthine dehydrogenase