Hermaphroditism Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0019269
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Genes

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

Symbol Name
AFM afamin
AKR1C1 aldo-keto reductase family 1, member C1
AKR1C2 aldo-keto reductase family 1, member C2
AKR1C3 aldo-keto reductase family 1, member C3
AR androgen receptor
CDIPT CDP-diacylglycerol--inositol 3-phosphatidyltransferase
CDK11B cyclin-dependent kinase 11B
CDK19 cyclin-dependent kinase 19
CELF3 CUGBP, Elav-like family member 3
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
DMRT1 doublesex and mab-3 related transcription factor 1
FBXW7 F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase
GFER growth factor, augmenter of liver regeneration
GPN1 GPN-loop GTPase 1
HSD17B3 hydroxysteroid (17-beta) dehydrogenase 3
HSP90B1 heat shock protein 90kDa beta (Grp94), member 1
LHCGR luteinizing hormone/choriogonadotropin receptor
MAPK15 mitogen-activated protein kinase 15
MECR mitochondrial trans-2-enoyl-CoA reductase
MNAT1 MNAT CDK-activating kinase assembly factor 1
NBEAL1 neurobeachin-like 1
NPR1 natriuretic peptide receptor 1
NPTXR neuronal pentraxin receptor
PEA15 phosphoprotein enriched in astrocytes 15
PKD2 polycystic kidney disease 2 (autosomal dominant)
PLSCR4 phospholipid scramblase 4
PRKD2 protein kinase D2
SGSM3 small G protein signaling modulator 3
SLC25A3 solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 3
SRY sex determining region Y
TRRAP transformation/transcription domain-associated protein
ZFPM2 zinc finger protein, FOG family member 2