Eyelid Xanthoma Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0155210
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Genes

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

Symbol Name
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5
ABCG8 ATP-binding cassette, sub-family G (WHITE), member 8
APOA2 apolipoprotein A-II
APOB apolipoprotein B
APOE apolipoprotein E
CD163 CD163 molecule
CEACAM5 carcinoembryonic antigen-related cell adhesion molecule 5
CYP27A1 cytochrome P450, family 27, subfamily A, polypeptide 1
EPHX2 epoxide hydrolase 2, cytoplasmic
G6PC glucose-6-phosphatase, catalytic subunit
GHR growth hormone receptor
GPC1 glypican 1
JPH3 junctophilin 3
LDLR low density lipoprotein receptor
PPP1R17 protein phosphatase 1, regulatory subunit 17
PTGS1 prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
SLC37A4 solute carrier family 37 (glucose-6-phosphate transporter), member 4
TTPA tocopherol (alpha) transfer protein