abnormal lower motor neuron morphology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any structural anomaly of the lower motor neuron. (Human Phenotype Ontology, HP_0002366)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002366
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Genes

8 genes associated with the abnormal lower motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
C19ORF12 chromosome 19 open reading frame 12
C9ORF72 chromosome 9 open reading frame 72
DCTN1 dynactin 1
MATR3 matrin 3
PLEKHG5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5
SETX senataxin
SIGMAR1 sigma non-opioid intracellular receptor 1