Hepatitis D Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis delta virus, which is an incomplete virus that requires the helper function of Hepatitis B virus to replicate and only occurs among people who are infected with the Hepatitis B virus. The infection has_symptom fatigue, has_symptom lethargy, has_symptom anorexia, has_symptom nausea, has_symptom jaundice, has_symptom clay-colored stools, has_symptom dark urine, has_symptom changes in personality, has_symptom disturbances in sleep, has_symptom confusion, has_symptom abnormal behavior, has_symptom somnolence, and has_symptom coma. (Human Disease Ontology, DOID_2047)
External Link https://www.disgenet.org/browser/0/1/0/C0524911
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Genes

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

Symbol Name
ADAR adenosine deaminase, RNA-specific
ADARB1 adenosine deaminase, RNA-specific, B1
B3GAT1 beta-1,3-glucuronyltransferase 1
BCL2 B-cell CLL/lymphoma 2
CD9 CD9 molecule
CHDH choline dehydrogenase
CHP1 calcineurin-like EF-hand protein 1
CLTC clathrin, heavy chain (Hc)
CLU clusterin
CXCL11 chemokine (C-X-C motif) ligand 11
DCTN6 dynactin 6
DLL1 delta-like 1 (Drosophila)
EIF2AK2 eukaryotic translation initiation factor 2-alpha kinase 2
EPHA3 EPH receptor A3
FLT4 fms-related tyrosine kinase 4
GAPDH glyceraldehyde-3-phosphate dehydrogenase
GATA3 GATA binding protein 3
GPT glutamic-pyruvate transaminase (alanine aminotransferase)
GSTK1 glutathione S-transferase kappa 1
HLA-B major histocompatibility complex, class I, B
HSPG2 heparan sulfate proteoglycan 2
IFI27 interferon, alpha-inducible protein 27
IFIH1 interferon induced with helicase C domain 1
IFNA1 interferon, alpha 1
IFNA13 interferon, alpha 13
IFNA2 interferon, alpha 2
IFNB1 interferon, beta 1, fibroblast
IFNG interferon, gamma
IFNL3 interferon, lambda 3
IL10 interleukin 10
LTF lactotransferrin
MAP4K4 mitogen-activated protein kinase kinase kinase kinase 4
MYC v-myc avian myelocytomatosis viral oncogene homolog
NRSN1 neurensin 1
NUP98 nucleoporin 98kDa
PAEP progestagen-associated endometrial protein
PCNA proliferating cell nuclear antigen
PDIK1L PDLIM1 interacting kinase 1 like
PKD2L1 polycystic kidney disease 2-like 1
PRSS3 protease, serine, 3
PSMB6 proteasome (prosome, macropain) subunit, beta type, 6
PSMD9 proteasome (prosome, macropain) 26S subunit, non-ATPase, 9
SLC10A1 solute carrier family 10 (sodium/bile acid cotransporter), member 1
SLC35A2 solute carrier family 35 (UDP-galactose transporter), member A2
SLCO6A1 solute carrier organic anion transporter family, member 6A1
SOAT1 sterol O-acyltransferase 1
SSSCA1 Sjogren syndrome/scleroderma autoantigen 1
TGFB1 transforming growth factor, beta 1
TICAM2 toll-like receptor adaptor molecule 2
TMED2 transmembrane emp24 domain trafficking protein 2
TMED7 transmembrane emp24 protein transport domain containing 7
TMED7-TICAM2 TMED7-TICAM2 readthrough
TNFSF14 tumor necrosis factor (ligand) superfamily, member 14
TPPP tubulin polymerization promoting protein
UGGT1 UDP-glucose glycoprotein glucosyltransferase 1
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1
UGT1A10 UDP glucuronosyltransferase 1 family, polypeptide A10
UGT1A3 UDP glucuronosyltransferase 1 family, polypeptide A3
UGT1A4 UDP glucuronosyltransferase 1 family, polypeptide A4
UGT1A5 UDP glucuronosyltransferase 1 family, polypeptide A5
UGT1A6 UDP glucuronosyltransferase 1 family, polypeptide A6
UGT1A7 UDP glucuronosyltransferase 1 family, polypeptide A7
UGT1A8 UDP glucuronosyltransferase 1 family, polypeptide A8
UGT1A9 UDP glucuronosyltransferase 1 family, polypeptide A9
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor
YY1 YY1 transcription factor