Amyotrophy, Monomelic Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1865384
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Genes

15 genes associated with the disease Amyotrophy, Monomelic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AIFM1 apoptosis-inducing factor, mitochondrion-associated, 1
C5ORF42 chromosome 5 open reading frame 42
CCL11 chemokine (C-C motif) ligand 11
CCL2 chemokine (C-C motif) ligand 2
CCL5 chemokine (C-C motif) ligand 5
CEP126 centrosomal protein 126kDa
DNAJB2 DnaJ (Hsp40) homolog, subfamily B, member 2
GARS glycyl-tRNA synthetase
SMN1 survival of motor neuron 1, telomeric
SMN2 survival of motor neuron 2, centromeric
SNRPN small nuclear ribonucleoprotein polypeptide N
SNURF SNRPN upstream reading frame
SOD1 superoxide dismutase 1, soluble
STMN1 stathmin 1
UCN urocortin