decreased circulating calcium level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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35 gene mutations causing the decreased circulating calcium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
ACSL4 acyl-CoA synthetase long-chain family member 4
ARID4A AT rich interactive domain 4A (RBP1-like)
CASR calcium-sensing receptor
CLDN4 claudin 4
CUL7 cullin 7
CYB561 cytochrome b561
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
DDOST dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit (non-catalytic)
FAM20C family with sequence similarity 20, member C
GCM2 glial cells missing homolog 2 (Drosophila)
GNAS GNAS complex locus
IL6ST interleukin 6 signal transducer
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
LYPD3 LY6/PLAUR domain containing 3
MED11 mediator complex subunit 11
MGAT2 mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
PHEX phosphate regulating endopeptidase homolog, X-linked
PITPNM1 phosphatidylinositol transfer protein, membrane-associated 1
PLVAP plasmalemma vesicle associated protein
PPP3CA protein phosphatase 3, catalytic subunit, alpha isozyme
PTH parathyroid hormone
RNF7 ring finger protein 7
SAG S-antigen; retina and pineal gland (arrestin)
SCGB1A1 secretoglobin, family 1A, member 1 (uteroglobin)
SLC34A2 solute carrier family 34 (type II sodium/phosphate cotransporter), member 2
SLC38A10 solute carrier family 38, member 10
TFAP2B transcription factor AP-2 beta (activating enhancer binding protein 2 beta)
TMEM189 transmembrane protein 189
TOX3 TOX high mobility group box family member 3
TRPV5 transient receptor potential cation channel, subfamily V, member 5
USP24 ubiquitin specific peptidase 24
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor
WWOX WW domain containing oxidoreductase
XPNPEP1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble