Gene table: search width pubmed_id = 23453667


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

protein
All allelic disease phenotypes - locus/disease symbols
Muscular dystrophy-dystroglycanopathy (Congenital with brain and eyes anomlies), type A11 - (AR)
2.28
23453667
B3GALNT2 (1q42.3)
Beta-1,3-N-acetylgalacto-saminyltransferase 2
* Congenital muscular dystrophy with hypoglycosylation of dystroglycan WWWS/MEB li - MDDGA11