Adrenal Hyperplasia, Congenital Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

21 genes associated with the Adrenal Hyperplasia, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
AR androgen receptor
C4A complement component 4A (Rodgers blood group)
C4B complement component 4B (Chido blood group)
CAPN10 calpain 10
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2
CYP21A1P cytochrome P450, family 21, subfamily A, polypeptide 1 pseudogene
CYP21A2 cytochrome P450, family 21, subfamily A, polypeptide 2
HLA-B major histocompatibility complex, class I, B
HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IGF2 insulin-like growth factor 2
IRS1 insulin receptor substrate 1
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
PON1 paraoxonase 1
POR P450 (cytochrome) oxidoreductase
PRKACA protein kinase, cAMP-dependent, catalytic, alpha
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B