hyperpituitarism Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010514
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Genes

31 genes associated with the hyperpituitarism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
AIP aryl hydrocarbon receptor interacting protein
AR androgen receptor
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CAV1 caveolin 1, caveolae protein, 22kDa
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CNBP CCHC-type zinc finger, nucleic acid binding protein
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
DCAF17 DDB1 and CUL4 associated factor 17
FMR1 fragile X mental retardation 1
FOS FBJ murine osteosarcoma viral oncogene homolog
FOXL2 forkhead box L2
FSHR follicle stimulating hormone receptor
GNAS GNAS complex locus
HFM1 HFM1, ATP-dependent DNA helicase homolog (S. cerevisiae)
HPGD hydroxyprostaglandin dehydrogenase 15-(NAD)
HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4
INSR insulin receptor
LHCGR luteinizing hormone/choriogonadotropin receptor
MEN1 multiple endocrine neoplasia I
NKX2-1 NK2 homeobox 1
PAX8 paired box 8
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
SECISBP2 SECIS binding protein 2
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
SLCO2A1 solute carrier organic anion transporter family, member 2A1
SMARCAL1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
SSTR5 somatostatin receptor 5
STAG3 stromal antigen 3
THRB thyroid hormone receptor, beta
TSHR thyroid stimulating hormone receptor