Gene table: search width pubmed_id = 40410591


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 associated with ptosis - (AR)
3.63
40410591
FOXK2 (17q25.3)
Forkhead box K2
* Congenital myopathy associated with ptosis