motor neuron atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Wasting involving the motor neuron. (Human Phenotype Ontology, HP_0007373)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007373
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Genes

16 genes associated with the motor neuron atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
ASAH1 N-acylsphingosine amidohydrolase (acid ceramidase) 1
C9ORF72 chromosome 9 open reading frame 72
FIG4 FIG4 phosphoinositide 5-phosphatase
IGHMBP2 immunoglobulin mu binding protein 2
MAPT microtubule-associated protein tau
MATR3 matrin 3
PFN1 profilin 1
PSEN1 presenilin 1
SETX senataxin
SMN1 survival of motor neuron 1, telomeric
SOD1 superoxide dismutase 1, soluble
TFG TRK-fused gene
UBA1 ubiquitin-like modifier activating enzyme 1
UBQLN2 ubiquilin 2
VRK1 vaccinia related kinase 1