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MIRAGE
cerebellar ataxia

Summary
Definition
A hereditary ataxia that is characterized by ataxia originating in the cerebellum.
Super Class
cerebellar disease hereditary ataxia
Disease Ontology
DOID:0050753
Mondo Disease Ontology
MeSH
MGI genotype (from TogoID)
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
23322 RPGRIP1L RPGRIP1 like
23345 SYNE1 spectrin repeat containing nuclear envelope protein 1
79944 L2HGDH L-2-hydroxyglutarate dehydrogenase
Displaying 1 entry
Gene ID Gene Symbol Description Source
12286 Cacna1a calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
Related Glycoprotein
Displaying all 2 entries
UniProt ID Protein Name Source
Q68CZ1 Protein fantom
Q8NF91 Nesprin-1
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: August 4, 2025