bull's eye maculopathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Progressive maculopathy characterized by concentric regions of hyper- and hypo-pigmentation. (Human Phenotype Ontology, HP_0011504)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011504
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4 genes associated with the bull's eye maculopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4
CNGB3 cyclic nucleotide gated channel beta 3
RIMS1 regulating synaptic membrane exocytosis 1
TMCO1 transmembrane and coiled-coil domains 1