cerebellar ataxia type 41

Summary
Synonym
  • SCA41
Definition
An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the TRPC3 gene on chromosome 4q27.
Super Class
autosomal dominant cerebellar ataxia
Disease Ontology
DOID:0111744
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7222 TRPC3 transient receptor potential cation channel subfamily C member 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
22065 Trpc3 transient receptor potential cation channel, subfamily C, member 3

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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