Sclerosis Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

26 genes associated with the Sclerosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
APOE apolipoprotein E
AQP4 aquaporin 4
C9ORF72 chromosome 9 open reading frame 72
F13A1 coagulation factor XIII, A1 polypeptide
GABBR1 gamma-aminobutyric acid (GABA) B receptor, 1
GABRA1 gamma-aminobutyric acid (GABA) A receptor, alpha 1
GABRA6 gamma-aminobutyric acid (GABA) A receptor, alpha 6
GABRB2 gamma-aminobutyric acid (GABA) A receptor, beta 2
GABRG2 gamma-aminobutyric acid (GABA) A receptor, gamma 2
GRN granulin
HTR1B 5-hydroxytryptamine (serotonin) receptor 1B, G protein-coupled
HTRA1 HtrA serine peptidase 1
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KCNMB4 potassium channel subfamily M regulatory beta subunit 4
MVP major vault protein
PRNP prion protein
SCN1A sodium channel, voltage gated, type I alpha subunit
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
TARDBP TAR DNA binding protein
TMEM106B transmembrane protein 106B
TPH1 tryptophan hydroxylase 1