Gene table: search width pubmed_id = 17322883


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

protein
All allelic disease phenotypes - locus/disease symbols
Spastic paraplegia 11, autosomal recessive - (AR)
15.22
10408536
16699786
17322883
SPG11 (15q21.1)
Spatacsin
* Spastic paraplegia 11 - SPG11
* Charcot-Marie-Tooth neuropathy Type 2X - CMT2X
* Amyotrophic lateral sclerosis 5 - ALS5