Gene table: search width pubmed_id = 19061983


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
Spastic paraplegia 42, autosomal dominant - (AD)
15.20
19061983
SLC33A1 (3q25.3)
Solute carrier family 33 (acetyl- CoA transporter)
* Spastic paraplegia 42, autosomal dominant - SPG42