Gene table: search width pubmed_id = 15635080


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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 26, autosomal recessive - (AR)
15.39
15635080
23746551
B4GALNT1 (12q13.3)
Beta-1,4-N-acetyl-galactosaminyl transferase 1
* Spastic paraplegia 26 - SPG26
* Charcot-Marie-Tooth disease, axonal