Amyotrophic lateral sclerosis Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing. (Human Disease Ontology, DOID_332)
External Link https://www.ebi.ac.uk/gwas/search?query=Amyotrophic lateral sclerosis
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Genes

25 genes associated with the Amyotrophic lateral sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
UNC13A unc-13 homolog A (C. elegans) 0.793579
SUSD2 sushi domain containing 2 0.499091
LOC102724192 0.449549
KIFAP3 kinesin-associated protein 3 0.405958
TIAM1 T-cell lymphoma invasion and metastasis 1 0.389385
DPP6 dipeptidyl-peptidase 6 0.369252
KIAA0513 KIAA0513 0.266721
STK36 serine/threonine kinase 36 0.255654
LAMA3 laminin, alpha 3 0.246511
C4ORF36 chromosome 4 open reading frame 36 0.22914
B4GALT6 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 6 0.220915
C9ORF72 chromosome 9 open reading frame 72 0.129504
ITPR2 inositol 1,4,5-trisphosphate receptor, type 2 0.129504
SELL selectin L 0.104568
ATXN1 ataxin 1 0.104568
ZFP64 ZFP64 zinc finger protein 0.085234
SUSD1 sushi domain containing 1 0.070053
CNTN4 contactin 4 0.057619
CPNE4 copine IV 0.057619
OR52K3P olfactory receptor, family 52, subfamily K, member 3 pseudogene 0.057619
LOC101927212 0.048624
MORN2 MORN repeat containing 2 0.048624
NT5C1A 5'-nucleotidase, cytosolic IA 0.048624
SLC39A11 solute carrier family 39, member 11 0.048624
FHDC1 FH2 domain containing 1 0.042592