Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1636
Gene Symbol: ACE
ACE
0.100 GeneticVariation disease BEFREE This meta-analysis indicates that the ACE I/D polymorphism is not associated with susceptibility to MS in Europeans of Slavic origin. 27568030 2016
Entrez Id: 1636
Gene Symbol: ACE
ACE
0.100 GeneticVariation disease BEFREE The ACE-I/D polymorphism does not contribute either to risk for nicotine dependence or to smoking severity among MS patients. 28127518 2017
Entrez Id: 1636
Gene Symbol: ACE
ACE
0.100 AlteredExpression disease BEFREE Published research has described increased expression of AT1R and ACE in tissues from MS patients and in animal models of MS such as experimental autoimmune encephalomyelitis (EAE). 31828731 2019
Entrez Id: 59272
Gene Symbol: ACE2
ACE2
0.010 AlteredExpression disease BEFREE ACE levels in CSF were lower in patients with NMO/NMOs (34.3+/-5.61 ng/ml) than in MS patients (42.5+/-8.19 ng/ml, P(corr)=0.035) and controls (44.7+/-4.02 ng/ml, P(corr)<0.0003) while ACE2 levels were lower in NMO/NMOs (1.13+/-0.49 ng/ml) and MS (1.75+/-0.86 ng/ml) patients than in controls (2.76+/-0.23 ng/ml, P(corr)<0.001 for both). 20541774 2010
Entrez Id: 43
Gene Symbol: ACHE
ACHE
0.020 GeneticVariation disease BEFREE Butyrylcholinesterase and Acetylcholinesterase polymorphisms in Multiple Sclerosis patients: implication in peripheral inflammation. 29358722 2018
Entrez Id: 43
Gene Symbol: ACHE
ACHE
0.020 Biomarker disease BEFREE Examining the effectiveness of acetylcholinesterase inhibitors and stimulant-based medications for cognitive dysfunction in multiple sclerosis: A systematic review and meta-analysis. 29406017 2018
Entrez Id: 2532
Gene Symbol: ACKR1
ACKR1
0.010 AlteredExpression disease BEFREE Here we show that during experimental autoimmune encephalomyelitis, an animal model of multiple sclerosis, the expression of DARC is upregulated at the blood-brain barrier. 24625696 2014
Entrez Id: 1238
Gene Symbol: ACKR2
ACKR2
0.020 AlteredExpression disease BEFREE Our data clearly show a decreased ACKR2 mRNA expression on PBMCs and increased plasma IL-33 levels of patients with MS. 31770664 2019
Entrez Id: 1238
Gene Symbol: ACKR2
ACKR2
0.020 Biomarker disease BEFREE Concordant to evidence in multiple sclerosis experimental models, our data corroborate a distinct role for ACKR2 in cerebral inflammatory processes compared to its reported functions in peripheral tissues. 29176798 2017
Entrez Id: 57007
Gene Symbol: ACKR3
ACKR3
0.030 Biomarker disease BEFREE The interaction between oxysterols and the G protein-coupled receptor Epstein-Barr virus-induced gene 2 (EBI2) fine-tunes immune cell migration, a mechanism efficiently targeted by several disease-modifying treatments developed to treat multiple sclerosis (MS), such as natalizumab. 28052250 2017
Entrez Id: 57007
Gene Symbol: ACKR3
ACKR3
0.030 Biomarker disease BEFREE Furthermore, this review provides potential therapeutic strategies for myelin repair by analyzing the relevance between the pathological changes and the regulatory roles of CXCL12/CXCR4/CXCR7 during MS. 29283028 2017
Entrez Id: 57007
Gene Symbol: ACKR3
ACKR3
0.030 GeneticVariation disease BEFREE Here, after performing whole exome sequencing, we found a MS patient harboring a rare and homozygous single nucleotide variant (SNV; rs61745847) of the G-protein coupled receptor (GPCR) galanin-receptor 2 (GALR2) that alters an important amino acid in the TM6 molecular toggle switch region (W249L). 30131588 2019
Entrez Id: 50
Gene Symbol: ACO2
ACO2
0.010 AlteredExpression disease BEFREE Mitochondrial aconitase activity was higher in MS patients than in controls (P < 0.05). 23761047 2014
Entrez Id: 55856
Gene Symbol: ACOT13
ACOT13
0.010 Biomarker disease BEFREE Although these data do not support a hypothesis that there is a role for these two HHVs in the pathogenesis of MS, nevertheless it may be suggested that (1) the two viruses possess strong neurotropism and the central nervous system seems to be a reservoir for them (2) HHV-6 infection is probably not transmitted maternally, but is acquired later in infancy. 9266465 1997
Entrez Id: 11332
Gene Symbol: ACOT7
ACOT7
0.010 Biomarker disease BEFREE Using mixed methods case-series evaluation in the development of a guided self-management hybrid CBT and ACT intervention for multiple sclerosis pain. 27557625 2017
Entrez Id: 60
Gene Symbol: ACTB
ACTB
0.010 AlteredExpression disease BEFREE These processes are crucial for the T-cells' ability to mediate inflammatory processes in autoimmune diseases such as MS. RhoA is a ubiquitously expressed small GTPase well described as a regulator of the actin cytoskeleton. 29904389 2018
Entrez Id: 345651
Gene Symbol: ACTBL2
ACTBL2
0.010 Biomarker disease BEFREE Using mixed methods case-series evaluation in the development of a guided self-management hybrid CBT and ACT intervention for multiple sclerosis pain. 27557625 2017
Entrez Id: 71
Gene Symbol: ACTG1
ACTG1
0.010 Biomarker disease BEFREE Using mixed methods case-series evaluation in the development of a guided self-management hybrid CBT and ACT intervention for multiple sclerosis pain. 27557625 2017
Entrez Id: 72
Gene Symbol: ACTG2
ACTG2
0.010 Biomarker disease BEFREE Using mixed methods case-series evaluation in the development of a guided self-management hybrid CBT and ACT intervention for multiple sclerosis pain. 27557625 2017
Entrez Id: 100
Gene Symbol: ADA
ADA
0.020 Biomarker disease BEFREE Multiple sclerosis should be included in differential diagnosis of disorders with ADA elevation in the CSF. 28427701 2017
Entrez Id: 100
Gene Symbol: ADA
ADA
0.020 AlteredExpression disease BEFREE A common database platform (tranSMART) for querying, analyzing and storing retrospective data of MS cohorts was set up to harmonize the data and compare results of ADA tests between different countries. 28170401 2017
Entrez Id: 132612
Gene Symbol: ADAD1
ADAD1
0.110 GeneticVariation disease BEFREE Our results did not show major influence of TENR-IL2-IL21 locus on susceptibility or disease progression in MS. 19523143 2009
Entrez Id: 132612
Gene Symbol: ADAD1
ADAD1
0.110 GeneticVariation disease GWASDB Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364 2011
Entrez Id: 6868
Gene Symbol: ADAM17
ADAM17
0.030 AlteredExpression disease LHGDN Further studies into the functional role of ADAM-17 in the pathogenesis of MS and other inflammatory conditions are required. 16900751 2006
Entrez Id: 6868
Gene Symbol: ADAM17
ADAM17
0.030 AlteredExpression disease BEFREE ADAM-17 expression is localised to endothelial cells in the human central nervous system (CNS) and is increased in multiple sclerosis (MS) white matter, suggesting a role in MS pathogenesis. 19324423 2009