hepatitis d Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
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)
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Genes

41 genes co-occuring with the disease hepatitis d in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
HBE1 hemoglobin, epsilon 1 1.65834
SLC35A2 solute carrier family 35 (UDP-galactose transporter), member A2 1.23473
IFNA2 interferon, alpha 2 1.17035
CYP2D7 cytochrome P450, family 2, subfamily D, polypeptide 7 (gene/pseudogene) 1.07698
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6 1.06564
IFNA17 interferon, alpha 17 0.963728
B3GAT2 beta-1,3-glucuronyltransferase 2 0.928346
EIF2AK2 eukaryotic translation initiation factor 2-alpha kinase 2 0.886799
GOT1 glutamic-oxaloacetic transaminase 1, soluble 0.856087
GOT2 glutamic-oxaloacetic transaminase 2, mitochondrial 0.824538
IFNA21 interferon, alpha 21 0.756971
MUT methylmalonyl CoA mutase 0.672722
PRKD3 protein kinase D3 0.67113
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9 0.631598
REXO1L1P REX1, RNA exonuclease 1 homolog (S. cerevisiae)-like 1, pseudogene 0.595233
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2 0.52729
AFP alpha-fetoprotein 0.507273
IFNA1 interferon, alpha 1 0.485505
SLC10A1 solute carrier family 10 (sodium/bile acid cotransporter), member 1 0.430768
SRF serum response factor (c-fos serum response element-binding transcription factor) 0.42814
FBN2 fibrillin 2 0.410161
UGT1A3 UDP glucuronosyltransferase 1 family, polypeptide A3 0.403064
PPIA peptidylprolyl isomerase A (cyclophilin A) 0.392629
CYP2A6 cytochrome P450, family 2, subfamily A, polypeptide 6 0.391141
IFNA10 interferon, alpha 10 0.378143
UGT1A10 UDP glucuronosyltransferase 1 family, polypeptide A10 0.374438
UGT1A8 UDP glucuronosyltransferase 1 family, polypeptide A8 0.373698
UGT1A5 UDP glucuronosyltransferase 1 family, polypeptide A5 0.371477
UGT1A4 UDP glucuronosyltransferase 1 family, polypeptide A4 0.369628
TAGLN transgelin 0.348981
UGT1A7 UDP glucuronosyltransferase 1 family, polypeptide A7 0.348246
UGT1A9 UDP glucuronosyltransferase 1 family, polypeptide A9 0.346409
ALB albumin 0.322637
HDAC2 histone deacetylase 2 0.307757
GGT1 gamma-glutamyltransferase 1 0.226952
C6ORF25 chromosome 6 open reading frame 25 0.219057
F2 coagulation factor II (thrombin) 0.200006
HLA-A major histocompatibility complex, class I, A 0.1936
NELFCD negative elongation factor complex member C/D 0.173832
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1 0.160948
F8 coagulation factor VIII, procoagulant component 0.157765