abnormality of the spinocerebellar tracts Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the spinocerebellar tracts, a set of axonal fibers originating in the spinal cord and terminating in the ipsilateral cerebellum. The spinocerebellar tract convey information to the cerebellum about limb and joint position (proprioception). They comprise the ventral spinocerebellar tract (FMA:72642), the anterior spinocerebellar tract (FMA:72642), and the posterior spinocerebellar tract (FMA:72641). (Human Phenotype Ontology, HP_0003133)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003133
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Genes

6 genes associated with the abnormality of the spinocerebellar tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATXN1 ataxin 1
ATXN2 ataxin 2
ATXN3 ataxin 3
GCLC glutamate-cysteine ligase, catalytic subunit
MAN2B1 mannosidase, alpha, class 2B, member 1
PLP1 proteolipid protein 1