amyotrophic lateral sclerosis; anoxia; Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group neurological (Genetic Association Database)
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Genes

25 genes associated with the disease amyotrophic lateral sclerosis; anoxia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACTR5 ARP5 actin-related protein 5 homolog (yeast)
ANG angiogenin, ribonuclease, RNase A family, 5
ANGPTL4 angiopoietin-like 4
CAV1 caveolin 1, caveolae protein, 22kDa
CP ceruloplasmin (ferroxidase)
HGF hepatocyte growth factor (hepapoietin A; scatter factor)
IL18BP interleukin 18 binding protein
INHBA inhibin, beta A
LEP leptin
MIF macrophage migration inhibitory factor (glycosylation-inhibiting factor)
MMP1 matrix metallopeptidase 1
MMP12 matrix metallopeptidase 12
PDGFB platelet-derived growth factor beta polypeptide
PGF placental growth factor
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
RECK reversion-inducing-cysteine-rich protein with kazal motifs
ROBO4 roundabout, axon guidance receptor, homolog 4 (Drosophila)
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SPP1 secreted phosphoprotein 1
STC1 stanniocalcin 1
STC2 stanniocalcin 2
TGFB1 transforming growth factor, beta 1
TYMP thymidine phosphorylase
WNT10B wingless-type MMTV integration site family, member 10B
WNT5A wingless-type MMTV integration site family, member 5A