Gene table: search width pubmed_id = 29528531


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 18A7, autosomal dominant - (AD)
15.10
29528531
ERLIN2 (8p12-p11.21)
ER lipid raft associated 2
* Spastic paraplegia 18 - SPG18
* Spastic paraplegia 18A7, autosomal dominant - SPG18A