Retinal Artery Occlusion Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D015356
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Genes

11 genes/proteins associated with the disease Retinal Artery Occlusion from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CASP3 caspase 3, apoptosis-related cysteine peptidase 1.18424
CRIP2 cysteine-rich protein 2 1.10699
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) 1.09226
HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) 1.06406
ARNTL aryl hydrocarbon receptor nuclear translocator-like 1.05828
MAPK10 mitogen-activated protein kinase 10 1.05052
AKT1 v-akt murine thymoma viral oncogene homolog 1 1.03976
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8) 1.03715
ATP5A1 ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1, cardiac muscle 1.02933
IL6 interleukin 6 1.02559
FGF2 fibroblast growth factor 2 (basic) 1.01361