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
Similar Terms
Downloads & Tools

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