Gangliosidoses, Gm2 Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0268274
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Genes

18 genes associated with the disease Gangliosidoses, Gm2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CLN3 ceroid-lipofuscinosis, neuronal 3
GLB1 galactosidase, beta 1
GM2A GM2 ganglioside activator
HEXA hexosaminidase A (alpha polypeptide)
HEXB hexosaminidase B (beta polypeptide)
HEXDC hexosaminidase (glycosyl hydrolase family 20, catalytic domain) containing
HHEX hematopoietically expressed homeobox
IGFALS insulin-like growth factor binding protein, acid labile subunit
OGA O-GlcNAcase
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
SYN1 synapsin I
TPP1 tripeptidyl peptidase I
UGT8 UDP glycosyltransferase 8