Gene table: search width pubmed_id = 14981520


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

protein
All allelic disease phenotypes - locus/disease symbols
Neuronopathy, distal hereditary motor, autosomal dominant 13 - (AD)
12.36
14981520
BSCL2 (11q12-q13.5)
Seipin
* Spastic paraplegia 17 - SPG17
* Neuronopathy, distal hereditary motor, autosomal dominant 13 - HMND13