Gene table: search width pubmed_id = 7825577


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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 6, autosomal dominant - (AD)
15.3
14508710
7825577
NIPA1 (15q11.2)
Non-imprinted in Prader-Willi/Angelman syndrome 1
* Spastic paraplegia 6 uncomplicated,autosomal dominant,Strumpell-Lorrain type - SPG6