macular degeneration Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
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)
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30 genes involed in the disease macular degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4
APOE apolipoprotein E
ASPM asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
BEST1 bestrophin 1
C2 complement component 2
C3 complement component 3
C9 complement component 9
CETP cholesteryl ester transfer protein, plasma
CFB complement factor B
CFH complement factor H
CFHR2 complement factor H-related 2
CFHR4 complement factor H-related 4
CFHR5 complement factor H-related 5
CFI complement factor I
CNGB3 cyclic nucleotide gated channel beta 3
CST3 cystatin C
CX3CR1 chemokine (C-X3-C motif) receptor 1
ELOVL4 ELOVL fatty acid elongase 4
ERCC6 excision repair cross-complementation group 6
F13B coagulation factor XIII, B polypeptide
FBLN5 fibulin 5
HMCN1 hemicentin 1
HTRA1 HtrA serine peptidase 1
LIPC lipase, hepatic
MAP2 microtubule-associated protein 2
PROM1 prominin 1
PRPH2 peripherin 2 (retinal degeneration, slow)
RAX2 retina and anterior neural fold homeobox 2
TIMP3 TIMP metallopeptidase inhibitor 3
TLR4 toll-like receptor 4