multiple system atrophy Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [LS]. (Human Disease Ontology, DOID_4752)
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Genes

22 genes associated with the disease multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ADH7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide
CXCL8 chemokine (C-X-C motif) ligand 8
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
EIF4EBP1 eukaryotic translation initiation factor 4E binding protein 1
ETV6 ets variant 6
FRAXA fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation)
GBA glucosidase, beta, acid
ICAM1 intercellular adhesion molecule 1
IL10 interleukin 10
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
IL6 interleukin 6
MCPH1 microcephalin 1
MSX1 msh homeobox 1
PPP1R14C protein phosphatase 1, regulatory (inhibitor) subunit 14C
SERPINA3 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 3
SLC1A4 solute carrier family 1 (glutamate/neutral amino acid transporter), member 4
SNCA synuclein, alpha (non A4 component of amyloid precursor)
SQSTM1 sequestosome 1
TGFB1 transforming growth factor, beta 1
TNF tumor necrosis factor
UCHL1 ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)