Gene table: search width pubmed_id = 23483706


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 3, autosomal dominant (Strumpell disease) - (AD)
15.1
15517445
23483706
8252041
ATL1 (14q22.1)
Atlastin GTPase 1
* Neuropathy, hereditary sensory, type ID - HSN1D
* Spastic paraplegia 3, autosomal dominant (Strumpell disease) - SP3A