Gene table: search width pubmed_id = 10822439


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Spinocerebellar ataxia 31 - (AD)
13.29
10822439
19878914
BEAN1 (16q21)
Brain expressed, associated with Nedd42
TK2 (16q22-q23)
Thymidine kinase 2, mitochondrial(M)
* spinocerebellar ataxia-31 - SCA31
* Mitochondrial dna depletion syndrome, myopathic form - MTDPS3
* Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive, 3 - PEOB3