Gene table: search width pubmed_id = 1379744


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

protein
All allelic disease phenotypes - locus/disease symbols
Myotonia, recessive (Becker disease) - (AR)
6.4
1379744
CLCN1 (7q35)
Chloride channel 1, skeletal muscle (Thomsen disease, autosomal dominant)
* Myotonia recessive - CLC1
* Myotonia congenita, autosomal dominant, Thomsen disease - THD
* Myotonia congenita, autosomal recessive, Becker disease - MCR