Retinal Drusen Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_2569)
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Genes

10 genes associated with the Retinal Drusen phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
APOE apolipoprotein E
ARMS2 age-related maculopathy susceptibility 2
BFAR bifunctional apoptosis regulator
C2 complement component 2
C3 complement component 3
CFB complement factor B
CFH complement factor H
EFEMP1 EGF containing fibulin-like extracellular matrix protein 1
HTRA1 HtrA serine peptidase 1