Abnormal Upper Motor Neuron Morphology Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Any structural anomaly that affects the upper motor neuron. (Human Phenotype Ontology, HP_0002127)
External Link https://www.disgenet.org/browser/0/1/0/C4025723
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Genes

20 genes associated with the disease Abnormal Upper Motor Neuron Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALDH18A1 aldehyde dehydrogenase 18 family, member A1
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
C9ORF72 chromosome 9 open reading frame 72
CHCHD10 coiled-coil-helix-coiled-coil-helix domain containing 10
ERLIN2 ER lipid raft associated 2
FUS FUS RNA binding protein
GBE1 glucan (1,4-alpha-), branching enzyme 1
IFIH1 interferon induced with helicase C domain 1
MATR3 matrin 3
POLR3A polymerase (RNA) III (DNA directed) polypeptide A, 155kDa
POLR3B polymerase (RNA) III (DNA directed) polypeptide B
SETX senataxin
SIGMAR1 sigma non-opioid intracellular receptor 1
SPG11 spastic paraplegia 11 (autosomal recessive)
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
SQSTM1 sequestosome 1
TARDBP TAR DNA binding protein
TBK1 TANK-binding kinase 1
TYROBP TYRO protein tyrosine kinase binding protein
VCP valosin containing protein