abnormality of calcium-phosphate metabolism Gene Set
Genes
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
|
