Gene table: search width pubmed_id = 16701995


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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 impaired intellectual development), type B2 - (AR)
2.33
16701995
POMT2 (14q24.3)
Protein-O-mannosyltransferase 2
* Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), - MDDGA2
* Walker-Warburg syndrome - WWS
* Limb-girdle, muscular dystrophy, type 2n - LGMD2N
* Muscle-eye-brain disease - MEB