Gene table: search width pubmed_id = 23746549


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

protein
All allelic disease phenotypes - locus/disease symbols
Nemaline myopathy (NEM8) - (AR)
3.8
23746549
KLHL40 (2p22.1)
Kelch-like family member 40
* Severe autosomal-recessive nemaline myopathy - NEM8