Gene table: search width pubmed_id = 30770808


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 9A - (AR)
3.49
30770808
FXR1 (3q26.33)
FMR1 autosomal homolog
* Congenital myopathy 9A - CMYP9A
* Congenital myopathy 9B, proximal with minicore - CMYP9B