Gene table: search width pubmed_id = 27066570


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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 (Limb-girdle), type C8 - (AR)
1.52
27066570
POMGNT2 (3p22.1)
protein O-linked mannose N-acetylglucosaminyltransferase 2
* Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, - MDDGA8
* Walker-Warburg syndrome - WWS
* LGMDR24