Distal Upper Limb Amyotrophy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Muscular atrophy of distal arm muscles. (Human Phenotype Ontology, HP_0007149)
External Link https://www.disgenet.org/browser/0/1/0/C4021581
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Genes

8 genes associated with the disease Distal Upper Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
C5ORF42 chromosome 5 open reading frame 42
CEP126 centrosomal protein 126kDa
DYSF dysferlin
FLNC filamin C, gamma
GAN gigaxonin
GJB1 gap junction protein, beta 1, 32kDa
INF2 inverted formin, FH2 and WH2 domain containing
MATR3 matrin 3