Myotonic Dystrophy Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

12 genes associated with the Myotonic Dystrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
AR androgen receptor
ATN1 atrophin 1
ATXN1 ataxin 1
ATXN3 ataxin 3
CLCN1 chloride channel, voltage-sensitive 1
CNBP CCHC-type zinc finger, nucleic acid binding protein
DMPK dystrophia myotonica-protein kinase
FRAXA fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation)
FXN frataxin
HTT huntingtin
KCNN3 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 3
MBNL1 muscleblind-like splicing regulator 1