Upper Limb Amyotrophy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Muscular atrophy involving the muscles of the upper limbs. (Human Phenotype Ontology, HP_0009129)
External Link https://www.disgenet.org/browser/0/1/0/C4021523
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
ADSSL1 adenylosuccinate synthase like 1
ANO5 anoctamin 5
CYP7B1 cytochrome P450, family 7, subfamily B, polypeptide 1
GARS glycyl-tRNA synthetase
HSPB1 heat shock 27kDa protein 1
KIF5A kinesin family member 5A
KY kyphoscoliosis peptidase
MYH7 myosin, heavy chain 7, cardiac muscle, beta
NEFH neurofilament, heavy polypeptide