age related macular degeneration Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A degeneration of macula and posterior pole that is characterized by a loss of vision in the center of the visual field (the macula) resulting from damage to the retina and resulting in blurring of the sharp central vision. (Human Disease Ontology, DOID_10871)
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27 genes involed in the disease age related 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
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
RAX2 retina and anterior neural fold homeobox 2
TIMP3 TIMP metallopeptidase inhibitor 3
TLR4 toll-like receptor 4