Macular Degeneration Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A retinal degeneration characterized by gradual deterioration of light-sensing cells in the tissues at the back of the eye; symptoms include vision loss. (Human Disease Ontology, DOID_4448)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D008268
Similar Terms
Downloads & Tools

Genes

18 genes/proteins associated with the disease Macular Degeneration from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CFH complement factor H 2.88009
C3 complement component 3 2.88009
C9 complement component 9 2.88009
ARMS2 age-related maculopathy susceptibility 2 2.88009
C1QTNF5 C1q and tumor necrosis factor related protein 5 2.88009
TLR4 toll-like receptor 4 2.88009
SQSTM1 sequestosome 1 2.88009
RPGR retinitis pigmentosa GTPase regulator 2.88009
NMNAT1 nicotinamide nucleotide adenylyltransferase 1 2.88009
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4 2.88009
VEGFA vascular endothelial growth factor A 2.88009
APOE apolipoprotein E 2.88009
TNFRSF10A tumor necrosis factor receptor superfamily, member 10a 2.88009
ERCC6 excision repair cross-complementation group 6 2.88009
CFB complement factor B 2.88009
CFI complement factor I 2.88009
C2 complement component 2 2.88009
RPE65 retinal pigment epithelium-specific protein 65kDa 1.13177