Gene table: search width pubmed_id = 16717220


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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 2K - (AR)
1.31
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
* Walker-Warburg syndrome - WWS