hyperparathyroidism Gene Set
Genes
18 genes associated with the hyperparathyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ACTG2
|
actin, gamma 2, smooth muscle, enteric
|
|
AP2S1
|
adaptor-related protein complex 2, sigma 1 subunit
|
|
CASR
|
calcium-sensing receptor
|
|
CDC73
|
cell division cycle 73
|
|
CDKN1A
|
cyclin-dependent kinase inhibitor 1A (p21, Cip1)
|
|
CDKN1B
|
cyclin-dependent kinase inhibitor 1B (p27, Kip1)
|
|
CDKN2B
|
cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4)
|
|
CDKN2C
|
cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4)
|
|
CYP27B1
|
cytochrome P450, family 27, subfamily B, polypeptide 1
|
|
FOXI1
|
forkhead box I1
|
|
GNA11
|
guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
|
|
GNAS
|
GNAS complex locus
|
|
KCNJ10
|
potassium channel, inwardly rectifying subfamily J, member 10
|
|
MEN1
|
multiple endocrine neoplasia I
|
|
OCRL
|
oculocerebrorenal syndrome of Lowe
|
|
RET
|
ret proto-oncogene
|
|
SLC26A4
|
solute carrier family 26 (anion exchanger), member 4
|
|
VDR
|
vitamin D (1,25- dihydroxyvitamin D3) receptor
|
