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GENE - TERM ANNOTATION REPORT

RGD ID: 1317932
Species: Mus musculus
RGD Object: Gene
Symbol: Ano10
Name: anoctamin 10
Acc ID: DOID:0050999
Term: autosomal recessive spinocerebellar ataxia 10
Definition: An autosomal recessive cerebellar ataxia that is characterized by ataxia, dysarthria, nystagmus and marked cerebellar atrophy, has_material_basis_in mutation in the ANO10 gene. (DO)
Definition Source(s): https://www.omim.org/entry/613728 "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
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