Muscular Atrophy, Spinal Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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21 genes associated with the Muscular Atrophy, Spinal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ANG angiogenin, ribonuclease, RNase A family, 5
AR androgen receptor
ATN1 atrophin 1
ATXN1 ataxin 1
ATXN3 ataxin 3
C9ORF72 chromosome 9 open reading frame 72
CHMP2B charged multivesicular body protein 2B
DMPK dystrophia myotonica-protein kinase
FRAXA fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation)
FUS FUS RNA binding protein
FXN frataxin
HTT huntingtin
KEAP1 kelch-like ECH-associated protein 1
LIX1 Lix1 homolog (chicken)
NAIP NLR family, apoptosis inhibitory protein
NFE2L2 nuclear factor, erythroid 2-like 2
PVR poliovirus receptor
SMN1 survival of motor neuron 1, telomeric
SMN2 survival of motor neuron 2, centromeric
SOD1 superoxide dismutase 1, soluble
TARDBP TAR DNA binding protein