Gene table: search width pubmed_id = 16793270


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

protein
All allelic disease phenotypes - locus/disease symbols
Distal myopathy with myotilin defect - (AD)
4.16
16793270
9829275
MYOT (5q31)
Myotilin
* Myofibrillar myopathy, myotilin related - MFM3
* Spheroid body myopathy
* Muscular dystrophy, Limb-Girdle, type 1A - LGMD1A