Gene table: search width pubmed_id = 31217819


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

protein
All allelic disease phenotypes - locus/disease symbols
Congenital Myopathy related to TNPO3 - (AD)
3.61
31192305
31217819
TNPO3 (7q32.1-q32.2)
Transportin 3
* Muscular dystrophy, Limb-Girdle, Type 1F - LGMD1F
* Congenital Myopathy related to TNPO3