abnormal motor neuron morphology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any structural anomal that affects the motor neuron. (Human Phenotype Ontology, HP_0002450)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002450
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27 genes associated with the abnormal 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)
ASAH1 N-acylsphingosine amidohydrolase (acid ceramidase) 1
C19ORF12 chromosome 19 open reading frame 12
C9ORF72 chromosome 9 open reading frame 72
DCTN1 dynactin 1
FIG4 FIG4 phosphoinositide 5-phosphatase
GBE1 glucan (1,4-alpha-), branching enzyme 1
GLE1 GLE1 RNA export mediator
IGHMBP2 immunoglobulin mu binding protein 2
MAPT microtubule-associated protein tau
MATR3 matrin 3
PFN1 profilin 1
PLEKHG5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5
PNPLA6 patatin-like phospholipase domain containing 6
POLR3A polymerase (RNA) III (DNA directed) polypeptide A, 155kDa
PSEN1 presenilin 1
SCP2 sterol carrier protein 2
SETX senataxin
SIGMAR1 sigma non-opioid intracellular receptor 1
SMN1 survival of motor neuron 1, telomeric
SOD1 superoxide dismutase 1, soluble
TFG TRK-fused gene
TREM2 triggering receptor expressed on myeloid cells 2
TYROBP TYRO protein tyrosine kinase binding protein
UBA1 ubiquitin-like modifier activating enzyme 1
UBQLN2 ubiquilin 2
VRK1 vaccinia related kinase 1