abnormal upper motor neuron morphology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any structural anomaly that affects the upper motor neuron. (Human Phenotype Ontology, HP_0002127)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002127
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Genes

9 genes associated with the abnormal upper 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)
GBE1 glucan (1,4-alpha-), branching enzyme 1
MATR3 matrin 3
PNPLA6 patatin-like phospholipase domain containing 6
POLR3A polymerase (RNA) III (DNA directed) polypeptide A, 155kDa
SETX senataxin
SIGMAR1 sigma non-opioid intracellular receptor 1
TREM2 triggering receptor expressed on myeloid cells 2
TYROBP TYRO protein tyrosine kinase binding protein