Exfoliation Syndrome Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_13641)
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Genes

33 genes associated with the Exfoliation Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
APOE apolipoprotein E
CBS cystathionine-beta-synthase
CDKN2B-AS1 CDKN2B antisense RNA 1
CHRNA4 cholinergic receptor, nicotinic, alpha 4 (neuronal)
CLU clusterin
CNTNAP2 contactin associated protein-like 2
ELN elastin
FBN1 fibrillin 1
GSTM1 glutathione S-transferase mu 1
GSTP1 glutathione S-transferase pi 1
GSTT1 glutathione S-transferase theta 1
LOXL1 lysyl oxidase-like 1
LTBP2 latent transforming growth factor beta binding protein 2
MFAP2 microfibrillar-associated protein 2
MMP1 matrix metallopeptidase 1
MMP2 matrix metallopeptidase 2
MMP3 matrix metallopeptidase 3
MMP9 matrix metallopeptidase 9
MT-TL2 tRNA
MT-TT tRNA
MTHFD1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
MYOC myocilin, trabecular meshwork inducible glucocorticoid response
SIX1 SIX homeobox 1
SIX6 SIX homeobox 6
SOD2 superoxide dismutase 2, mitochondrial
TGFB1 transforming growth factor, beta 1
TGM2 transglutaminase 2
TLR4 toll-like receptor 4
TNF tumor necrosis factor