Gene table: search width pubmed_id = 15792865


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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 C1 - (AR)
1.46
15792865
16717220
POMT1 (9q34.1)
Protein-O-mannosyltransferase 1
* Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), - MDDGA1
* Muscular dystrophy, Limb-Girdle, type 2K - LGMD2K
* Muscular dystrophy-dystrooglycanopathy (congenital with mental retardation), type B1 - MDDGB1
* Walker-Warburg syndrome - WWS