Gene table: search width pubmed_id = 25205112


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Spinocerebellar ataxia, autosomal recessive 19 (Lichtenstein-Knorr syndrome) - (AR)
13.79
25205112
SLC9A1 (1p36.11)
Solute carrier family 9, member 1
* Spinocerebellar ataxia, autosomal recessive 19 - SCAR19