Gene table: search width pubmed_id = 21194679


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

protein
All allelic disease phenotypes - locus/disease symbols
Hereditary sensory neuropathy type ID - (AD)
14.97
21194679
ATL1 (14q22.1)
Atlastin GTPase 1
* Neuropathy, hereditary sensory, type ID - HSN1D
* Spastic paraplegia 3, autosomal dominant (Strumpell disease) - SP3A