Vitreoretinal Degeneration Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Gradual deterioration of the vitreous humor and retina. (Human Phenotype Ontology, HP_0000655)
External Link https://www.disgenet.org/browser/0/1/0/C0344290
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Genes

20 genes associated with the disease Vitreoretinal Degeneration 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
CAPN5 calpain 5
COL11A1 collagen, type XI, alpha 1
COL18A1 collagen, type XVIII, alpha 1
COL2A1 collagen, type II, alpha 1
COL9A1 collagen, type IX, alpha 1
COL9A2 collagen, type IX, alpha 2
COL9A3 collagen, type IX, alpha 3
CRB1 crumbs family member 1, photoreceptor morphogenesis associated
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
FBN1 fibrillin 1
FZD4 frizzled class receptor 4
KCNJ13 potassium channel, inwardly rectifying subfamily J, member 13
LOXL3 lysyl oxidase-like 3
LRP5 low density lipoprotein receptor-related protein 5
LRRC32 leucine rich repeat containing 32
NDP Norrie disease (pseudoglioma)
NR2E3 nuclear receptor subfamily 2, group E, member 3
TSPAN12 tetraspanin 12
VCAN versican