Gene table: search width pubmed_id = 17878207


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

protein
All allelic disease phenotypes - locus/disease symbols
Limb-Girdle, Muscular dystrophy, type 2O - (AR)
1.35
17878207
18195152
19067344
22419172
POMGNT1 (1p34.1)
O-linked mannose beta1,2-N-acetylglucosaminyltransferase
* Limb-girdle, muscular dystrophy, type 2o - LGMD2O
* Walker-Warburg syndrome - WWS
* Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type - MDDGB3
* Muscle-eye-brain disease - MEB
* Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), - MDDGA3