Atrophic Retina Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0521694
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Genes

23 genes associated with the disease Atrophic Retina 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
ARSG arylsulfatase G
C8ORF37 chromosome 8 open reading frame 37
CEP78 centrosomal protein 78kDa
CTSD cathepsin D
CYP4V2 cytochrome P450, family 4, subfamily V, polypeptide 2
FKRP fukutin related protein
FKTN fukutin
HGSNAT heparan-alpha-glucosaminide N-acetyltransferase
KDR kinase insert domain receptor
LAMA1 laminin, alpha 1
LARGE like-glycosyltransferase
OPA1 optic atrophy 1 (autosomal dominant)
PLXNA2 plexin A2
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
POMT1 protein-O-mannosyltransferase 1
POMT2 protein-O-mannosyltransferase 2
REEP6 receptor accessory protein 6
RPE ribulose-5-phosphate-3-epimerase
RS1 retinoschisin 1
SLC7A14 solute carrier family 7, member 14
STUB1 STIP1 homology and U-box containing protein 1, E3 ubiquitin protein ligase
VEGFA vascular endothelial growth factor A