Deficiency Of Steroid 21-Monooxygenase Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0268287
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Genes

50 genes associated with the disease Deficiency Of Steroid 21-Monooxygenase in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AR androgen receptor
ARR3 arrestin 3, retinal (X-arrestin)
BEST1 bestrophin 1
BRD2 bromodomain containing 2
C4A complement component 4A (Rodgers blood group)
C4B complement component 4B (Chido blood group)
C4B_2 complement component 4B (Chido blood group), copy 2
CAPN10 calpain 10
CASR calcium-sensing receptor
CFC1 cripto, FRL-1, cryptic family 1
CRH corticotropin releasing hormone
CXADR coxsackie virus and adenovirus receptor
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1
CYP21A2 cytochrome P450, family 21, subfamily A, polypeptide 2
CYP2B6 cytochrome P450, family 2, subfamily B, polypeptide 6
CYP2C19 cytochrome P450, family 2, subfamily C, polypeptide 19
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4
CYP3A7 cytochrome P450, family 3, subfamily A, polypeptide 7
CYP4F3 cytochrome P450, family 4, subfamily F, polypeptide 3
DKK1 dickkopf WNT signaling pathway inhibitor 1
DMD dystrophin
FPR2 formyl peptide receptor 2
GH1 growth hormone 1
GLO1 glyoxalase I
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
GRB7 growth factor receptor-bound protein 7
HLA-A major histocompatibility complex, class I, A
HLA-B major histocompatibility complex, class I, B
HLA-DOA major histocompatibility complex, class II, DO alpha
HSD17B1 hydroxysteroid (17-beta) dehydrogenase 1
HSD3B2 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2
IDS iduronate 2-sulfatase
IGF2 insulin-like growth factor 2
IRS1 insulin receptor substrate 1
NR1I2 nuclear receptor subfamily 1, group I, member 2
NR1I3 nuclear receptor subfamily 1, group I, member 3
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
NR3C2 nuclear receptor subfamily 3, group C, member 2
POMC proopiomelanocortin
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
TBL1XR1 transducin (beta)-like 1 X-linked receptor 1
TNC tenascin C
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11
TNXB tenascin XB
TRIM13 tripartite motif containing 13
TRIM27 tripartite motif containing 27