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spinocerebellar ataxia 44

Summary
Definition
An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the GRM1 gene on chromosome 6q24.
Super Class
autosomal dominant cerebellar ataxia
Disease Ontology
DOID:0080286
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
2911 GRM1 glutamate metabotropic receptor 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
14816 Grm1 glutamate receptor, metabotropic 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
24414 Grm1 glutamate metabotropic receptor 1
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: December 9, 2024