DDX58, DExD/H-box helicase 58, 23586

N. diseases: 144; N. variants: 10
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11795343
rs11795343
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C0033860
Disease:
Psoriasis
T 0.800 GeneticVariation GWASCAT Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility. 25903422 2015
dbSNP: rs11795343
rs11795343
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C0033860
Disease:
Psoriasis
T 0.800 GeneticVariation GWASCAT Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms. 25574825 2015
dbSNP: rs11795343
rs11795343
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C0033860
Disease:
Psoriasis
0.800 GeneticVariation GWASDB Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 23143594 2012
dbSNP: rs11795343
rs11795343
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C0033860
Disease:
Psoriasis
T 0.800 GeneticVariation GWASCAT Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 23143594 2012
dbSNP: rs786204847
rs786204847
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C4225380
Disease:
SINGLETON-MERTEN SYNDROME 2
G 0.800 CausalMutation CLINVAR
dbSNP: rs786204847
rs786204847
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C4225380
Disease:
SINGLETON-MERTEN SYNDROME 2
0.800 GeneticVariation UNIPROT
dbSNP: rs786204848
rs786204848
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C4225380
Disease:
SINGLETON-MERTEN SYNDROME 2
0.800 GeneticVariation UNIPROT
dbSNP: rs786204848
rs786204848
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C4225380
Disease:
SINGLETON-MERTEN SYNDROME 2
A 0.800 CausalMutation CLINVAR
dbSNP: rs7045087
rs7045087
Entrez Id: 48;23586
Gene Symbol: ACO1;DDX58
ACO1;DDX58
CUI: C0518015
Disease:
Hemoglobin measurement
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7045087
rs7045087
Entrez Id: 48;23586
Gene Symbol: ACO1;DDX58
ACO1;DDX58
CUI: C0018935
Disease:
Hematocrit procedure
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7045087
rs7045087
Entrez Id: 48;23586
Gene Symbol: ACO1;DDX58
ACO1;DDX58
CUI: C0014772
Disease:
Red Blood Cell Count measurement
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs9695310
rs9695310
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C0019196
Disease:
Hepatitis C
0.010 GeneticVariation BEFREE The current study genotyped two selected SNPs (IFIH1 rs3747517 and DDX58 rs9695310) using TaqMan allelic discrimination assay to assess their association with the susceptibility and clinical outcome of HCV infection among 3065 participants (1545 non-HCV infection individuals, 568 spontaneous HCV clearance cases, and 952 persistent infection patients). 30633820 2019
dbSNP: rs9695310
rs9695310
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C1861453
Disease:
Pseudohyperkalemia Cardiff
0.010 GeneticVariation BEFREE IFIH1 rs3747517 (dominant model: Adjusted odds ratio [OR] = 1.34, 95% confidence interval [CI] = 1.07-1.68; P = 0.009) and DDX58 rs9695310 (dominant model: Adjusted OR = 1.43, 95% CI = 1.15-1.78; P = 0.001) were associated with chronic hepatitis C (CHC). 30633820 2019
dbSNP: rs9695310
rs9695310
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C0524910
Disease:
Hepatitis C, Chronic
0.010 GeneticVariation BEFREE Genetic variations at IFIH1 rs3747517 and DDX58 rs9695310 were independent predictors of chronic hepatitis C in Chinese Han population. 30633820 2019
dbSNP: rs3739674
rs3739674
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C0018572
Disease:
Hand, Foot and Mouth Disease
0.010 GeneticVariation BEFREE The results indicated that RIG-1 (rs3739674 and rs9695310) polymorphisms are associated with an increased risk of EV71-induced HFMD in Chinese children, whereas RIG-1 rs3739674 and TLR3 rs5743305 polymorphisms are associated with disease severity. 29235129 2018
dbSNP: rs786204847
rs786204847
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C0004364
Disease:
Autoimmune Diseases
0.010 GeneticVariation BEFREE Mutations in RIG-I (C268F and E373A) lead to impaired ATPase activity, thereby driving hyperactive signaling associated with autoimmune diseases. 30560918 2018
dbSNP: rs786204848
rs786204848
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C0004364
Disease:
Autoimmune Diseases
0.010 GeneticVariation BEFREE Mutations in RIG-I (C268F and E373A) lead to impaired ATPase activity, thereby driving hyperactive signaling associated with autoimmune diseases. 30560918 2018
dbSNP: rs9695310
rs9695310
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C0018572
Disease:
Hand, Foot and Mouth Disease
0.010 GeneticVariation BEFREE The results indicated that RIG-1 (rs3739674 and rs9695310) polymorphisms are associated with an increased risk of EV71-induced HFMD in Chinese children, whereas RIG-1 rs3739674 and TLR3 rs5743305 polymorphisms are associated with disease severity. 29235129 2018
dbSNP: rs10813831
rs10813831
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C1333064
Disease:
Classical Hodgkin's Lymphoma
0.010 GeneticVariation BEFREE Toll-like receptors 9 (TLR9_rs5743836), and 3 (TLR3_rs3775291), Interleukin-28B (IL28B_rs12979860), and DEAD-box polypeptide 58 (DDX58_rs10813831) were genotyped in 73 EBV-positive and 106 EBV-negative cHL patients and 396 controls. 27267403 2017
dbSNP: rs10813831
rs10813831
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C2347747
Disease:
Adult Classical Hodgkin Lymphoma
0.010 GeneticVariation BEFREE Only DDX58_rs10813831 T-allele was decreased among EBV-positive cHL compared to controls. 27267403 2017
dbSNP: rs669260
rs669260
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C0019196
Disease:
Hepatitis C
0.010 GeneticVariation BEFREE SOCS1 rs243327, TLR9 rs352140, and RIG-I rs669260 polymorphisms might affect liver pathophysiology and the cirrhotic outcome following genotype 4 HCV infection. 28762092 2017
dbSNP: rs758594231
rs758594231
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C4086165
Disease:
Childhood Neuroblastoma
0.010 GeneticVariation BEFREE Marked dysregulations of microbial defense factors Ifit3 and Rsad2 were consistently observed upon five analyses: (1) Pink1 <sup>-/-</sup> primary neurons in the first weeks after brain dissociation, (2) aged Pink1 <sup>-/-</sup> midbrain with transgenic A53T-alpha-synuclein overexpression, (3) human neuroblastoma cells with PINK1-knockdown and murine Pink1 <sup>-/-</sup> embryonal fibroblasts undergoing acute starvation, (4) triggering mitophagy in these cells with trifluoromethoxy carbonylcyanide phenylhydrazone (FCCP), and (5) subjecting them to pathogenic RNA-analogue poly(I:C). 28768533 2017
dbSNP: rs758594231
rs758594231
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C0027819
Disease:
Neuroblastoma
0.010 GeneticVariation BEFREE Marked dysregulations of microbial defense factors Ifit3 and Rsad2 were consistently observed upon five analyses: (1) Pink1 <sup>-/-</sup> primary neurons in the first weeks after brain dissociation, (2) aged Pink1 <sup>-/-</sup> midbrain with transgenic A53T-alpha-synuclein overexpression, (3) human neuroblastoma cells with PINK1-knockdown and murine Pink1 <sup>-/-</sup> embryonal fibroblasts undergoing acute starvation, (4) triggering mitophagy in these cells with trifluoromethoxy carbonylcyanide phenylhydrazone (FCCP), and (5) subjecting them to pathogenic RNA-analogue poly(I:C). 28768533 2017
dbSNP: rs758594231
rs758594231
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C0700095
Disease:
Central neuroblastoma
0.010 GeneticVariation BEFREE Marked dysregulations of microbial defense factors Ifit3 and Rsad2 were consistently observed upon five analyses: (1) Pink1 <sup>-/-</sup> primary neurons in the first weeks after brain dissociation, (2) aged Pink1 <sup>-/-</sup> midbrain with transgenic A53T-alpha-synuclein overexpression, (3) human neuroblastoma cells with PINK1-knockdown and murine Pink1 <sup>-/-</sup> embryonal fibroblasts undergoing acute starvation, (4) triggering mitophagy in these cells with trifluoromethoxy carbonylcyanide phenylhydrazone (FCCP), and (5) subjecting them to pathogenic RNA-analogue poly(I:C). 28768533 2017
dbSNP: rs3205166
rs3205166
Entrez Id: 23586
Gene Symbol: DDX58
DDX58
CUI: C0011311
Disease:
Dengue Fever
0.010 GeneticVariation BEFREE The results revealed a lower carrier frequency of the DDX58 rs3205166 G allele in DEN than in HCs and a higher frequency of the DDX58 rs669260 T/C genotype in DHF than in DF cases (P = 0.043, OR with 95 % CI 3.358 [1.038-10.861]). 25850761 2015