abnormality of glycoprotein metabolism Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of a glycoprotein metabolic process. (Human Phenotype Ontology, HP_0004367)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0004367
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Genes

18 genes associated with the abnormality of glycoprotein metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
SHBG sex hormone-binding globulin 3.05395
JMJD1C jumonji domain containing 1C 2.32875
TP53 tumor protein p53 2.01845
FUT6 fucosyltransferase 6 (alpha (1,3) fucosyltransferase) 1.83896
GCKR glucokinase (hexokinase 4) regulator 1.79316
FUT8 fucosyltransferase 8 (alpha (1,6) fucosyltransferase) 1.24751
SLCO1B1 solute carrier organic anion transporter family, member 1B1 1.21853
BAIAP2L1 BAI1-associated protein 2-like 1 1.19958
HNF1A HNF1 homeobox A 1.18704
CD68 CD68 molecule 1.15352
SCUBE2 signal peptide, CUB domain, EGF-like 2 1.15352
CEP112 centrosomal protein 112kDa 1.0674
CDH4 cadherin 4, type 1, R-cadherin (retinal) 1.00059
SNED1 sushi, nidogen and EGF-like domains 1 0.969142
ROBO2 roundabout, axon guidance receptor, homolog 2 (Drosophila) 0.899912
FTO fat mass and obesity associated 0.855449
MGAT5 mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase 0.814376
B3GAT1 beta-1,3-glucuronyltransferase 1 0.549861