Gene table: search width pubmed_id = 25585697


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 30, autosomal dominant - (AD)
15.13
25585697
KIF1A (2q37.3)
Kinesin family member 1A
* Neuropathy, hereditary sensory, type IIC - HSN2C
* Spastic paraplegia 30 - SPG30