Gene table: search width pubmed_id = 40497796


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Congenital myopathy - (AR)
3.62
40497796
DST (6p12.1)
Dystonin
* Hereditary sensory and autonomic neuropathy type VI - HSAN6