Tay-Sachs Disease Gene Set
Genes
24 genes associated with the disease Tay-Sachs Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ARSA
|
arylsulfatase A
|
|
ASPA
|
aspartoacylase
|
|
CSF2
|
colony stimulating factor 2 (granulocyte-macrophage)
|
|
FBN1
|
fibrillin 1
|
|
FCGRT
|
Fc fragment of IgG, receptor, transporter, alpha
|
|
GBA
|
glucosidase, beta, acid
|
|
GJB2
|
gap junction protein, beta 2, 26kDa
|
|
GLB1
|
galactosidase, beta 1
|
|
GM2A
|
GM2 ganglioside activator
|
|
GRN
|
granulin
|
|
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
|
|
LAMC2
|
laminin, gamma 2
|
|
LAMP1
|
lysosomal-associated membrane protein 1
|
|
NEU3
|
sialidase 3 (membrane sialidase)
|
|
NPTX1
|
neuronal pentraxin I
|
|
OGA
|
O-GlcNAcase
|
|
POU5F1
|
POU class 5 homeobox 1
|
|
SEMA6A
|
sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A
|
|
SOD1
|
superoxide dismutase 1, soluble
|
|
UBR5
|
ubiquitin protein ligase E3 component n-recognin 5
|
