Morphological Abnormality Of The Pyramidal Tract Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Any structural abnormality of the pyramidal tract, whose chief element, the corticospinal tract, is the only direct connection between the brain and the spinal cord. In addition to the corticospinal tract, the pyramidal system includes the corticobulbar, corticomesencephalic, and corticopontine tracts. (Human Phenotype Ontology, HP_0002062)
External Link https://www.disgenet.org/browser/0/1/0/C4021761
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Genes

17 genes associated with the disease Morphological Abnormality Of The Pyramidal Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AIFM1 apoptosis-inducing factor, mitochondrion-associated, 1
ATXN10 ataxin 10
ATXN8 ataxin 8
CTC1 CTS telomere maintenance complex component 1
DPYS dihydropyrimidinase
GAN gigaxonin
KCNC3 potassium channel, voltage gated Shaw related subfamily C, member 3
L2HGDH L-2-hydroxyglutarate dehydrogenase
MAPT microtubule-associated protein tau
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator
SLC19A3 solute carrier family 19 (thiamine transporter), member 3
SLC25A15 solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
TREX1 three prime repair exonuclease 1
VAPB VAMP (vesicle-associated membrane protein)-associated protein B and C