chronic fatigue syndrome Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A syndrome that involves prolonged and severe tiredness or weariness that is unrelated to exertion, is not relieved by rest and for a minimum of six months and is not directly caused by other conditions. (Human Disease Ontology, DOID_8544)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:8544
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Genes

33 genes associated with the disease chronic fatigue syndrome in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
GRIK2 glutamate receptor, ionotropic, kainate 2 0.716372
PPFIBP1 PTPRF interacting protein, binding protein 1 (liprin beta 1) 0.668836
LILRB4 leukocyte immunoglobulin-like receptor, subfamily B (with TM and ITIM domains), member 4 0.668836
NLRP13 NLR family, pyrin domain containing 13 0.615118
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B 0.615118
LINC00309 long intergenic non-protein coding RNA 309 0.615118
HS6ST3 heparan sulfate 6-O-sulfotransferase 3 0.615118
CFL1P1 cofilin 1 (non-muscle) pseudogene 1 0.586345
KCNJ6 potassium channel, inwardly rectifying subfamily J, member 6 0.564734
TECTB tectorin beta 0.564734
KRT33A keratin 33A, type I 0.564734
OTOG otogelin 0.564734
CLYBL citrate lyase beta like 0.564734
FLJ41278 uncharacterized LOC400046 0.564734
RASGRF2 Ras protein-specific guanine nucleotide-releasing factor 2 0.547225
DTX4 deltex 4, E3 ubiquitin ligase 0.547225
MIR205HG MIR205 host gene 0.532547
MSH3 mutS homolog 3 0.532547
AFAP1 actin filament associated protein 1 0.532547
FBXO42 F-box protein 42 0.532547
FRA10AC1 fragile site, folic acid type, rare, fra(10)(q23.3) or fra(10)(q24.2) candidate 1 0.532547
MTAP methylthioadenosine phosphorylase 0.532547
NPAS2 neuronal PAS domain protein 2 0.520364
PIP5K1B phosphatidylinositol-4-phosphate 5-kinase, type I, beta 0.520364
NLRP11 NLR family, pyrin domain containing 11 0.510061
SIX6 SIX homeobox 6 0.510061
KLHL32 kelch-like family member 32 0.510061
SHFM1 split hand/foot malformation (ectrodactyly) type 1 0.510061
RNLS renalase, FAD-dependent amine oxidase 0.510061
MAGI3 membrane associated guanylate kinase, WW and PDZ domain containing 3 0.510061
SCN8A sodium channel, voltage gated, type VIII alpha subunit 0.502485
TCERG1 transcription elongation regulator 1 0.502485
ARHGAP20 Rho GTPase activating protein 20 0.502485
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