cerebellar ataxia type 47

Summary
Synonym
  • SCA47
Definition
An autosomal dominant cerebellar ataxia characterized by adult onset of slowly progressive cerebellar ataxia or in some cases earlier onset of ataxia accompanied by delayed motor development and short stature that has_material_basis_in heterozygous mutation in the PUM1 gene on chromosome 1p35.2.
Super Class
autosomal dominant cerebellar ataxia
Disease Ontology
DOID:0111743
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9698 PUM1 pumilio RNA binding family member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
80912 Pum1 pumilio RNA-binding family member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
850647 PUF3 mRNA-binding protein PUF3

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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