Gene table: search width pubmed_id = 14981520


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 17, autosomal dominant (Silver) - (AD)
15.9
14981520
BSCL2 (11q12-q13.5)
Seipin
* Neuronopathy, distal hereditary motor, type V - HMN5
* Spastic paraplegia 17 - SPG17