Blindness Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0750958
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Genes

23 genes associated with the disease Blindness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4
AMD1 adenosylmethionine decarboxylase 1
ATIC 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase
DOCK7 dedicator of cytokinesis 7
FGF2 fibroblast growth factor 2 (basic)
HLA-A major histocompatibility complex, class I, A
HLA-B major histocompatibility complex, class I, B
LCA5 Leber congenital amaurosis 5
LRP5 low density lipoprotein receptor-related protein 5
MDM2 MDM2 proto-oncogene, E3 ubiquitin protein ligase
MOG myelin oligodendrocyte glycoprotein
MYO7A myosin VIIA
OPA1 optic atrophy 1 (autosomal dominant)
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit beta
PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta
PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma
POLG polymerase (DNA directed), gamma
RPE65 retinal pigment epithelium-specific protein 65kDa
TCHP trichoplein, keratin filament binding
TIMM8A translocase of inner mitochondrial membrane 8 homolog A (yeast)
USH2A Usher syndrome 2A (autosomal recessive, mild)
VEGFA vascular endothelial growth factor A