Precocious Pubarche Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0342541
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Genes

30 genes associated with the disease Precocious Pubarche in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADRB3 adrenoceptor beta 3
AKR1C3 aldo-keto reductase family 1, member C3
AR androgen receptor
ATRX alpha thalassemia/mental retardation syndrome X-linked
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
CYP21A2 cytochrome P450, family 21, subfamily A, polypeptide 2
GAD2 glutamate decarboxylase 2 (pancreatic islets and brain, 65kDa)
HEY2 hes-related family bHLH transcription factor with YRPW motif 2
HSD17B7 hydroxysteroid (17-beta) dehydrogenase 7
HSD3B2 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2
IGF1 insulin-like growth factor 1 (somatomedin C)
IGF1R insulin-like growth factor 1 receptor
IGF2 insulin-like growth factor 2
IGFBP1 insulin-like growth factor binding protein 1
IRS1 insulin receptor substrate 1
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
MC4R melanocortin 4 receptor
MKRN3 makorin ring finger protein 3
NDUFB2 NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 2, 8kDa
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
PAPSS2 3'-phosphoadenosine 5'-phosphosulfate synthase 2
POMC proopiomelanocortin
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SHBG sex hormone-binding globulin
SORBS1 sorbin and SH3 domain containing 1
STK11 serine/threonine kinase 11
TBX1 T-box 1
TGM2 transglutaminase 2
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor