Gene table: search width pubmed_id = 19696032


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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 with axonal neuropathy type 2 - (AR)
13.95
14770181
19696032
SETX (9q34.13)
Senataxin
* Neuropathy, distal hereditary motor, with pyramidal features - ALS4
* Spinocerebellar ataxia, autosomal recessive 1 - SCAR1
* Spinocerebellar ataxia with axonal neuropathy type 2 - SCAN2