Gene table: search width pubmed_id = 20970104


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

protein
All allelic disease phenotypes - locus/disease symbols
Hypertrophic cardiomyopathy, 20 - (AD)
10.21
20970104
NEXN (1p32-p31 )
Nexilin(F-actin binding protein)
* Hypertrophic cardiomyopathy related to nexilin
* Cardiomyopathy, familial hypertrophic 20 - CMH20
* Cardiomyopathy, dilated, 1CC - CMD1CC