cerebellar vermis atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Wasting (atrophy) of the vermis of cerebellum. (Human Phenotype Ontology, HP_0006855)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006855
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5 genes associated with the cerebellar vermis atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1
KIF1A kinesin family member 1A
QARS glutaminyl-tRNA synthetase
SACS sacsin molecular chaperone