abnormality of calcium-phosphate metabolism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100530
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17 genes associated with the abnormality of calcium-phosphate metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIRE autoimmune regulator
CASR calcium-sensing receptor
CLDN19 claudin 19
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
FAM20A family with sequence similarity 20, member A
GCM2 glial cells missing homolog 2 (Drosophila)
GNAS GNAS complex locus
GNAS-AS1 GNAS antisense RNA 1
OCRL oculocerebrorenal syndrome of Lowe
PHEX phosphate regulating endopeptidase homolog, X-linked
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PTH1R parathyroid hormone 1 receptor
RET ret proto-oncogene
RNU4ATAC RNA, U4atac small nuclear (U12-dependent splicing)
SOST sclerostin
STX16 syntaxin 16
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor