vitamin e deficiency Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0100513
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Genes

22 genes associated with the vitamin e deficiency phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
CYP4F2 cytochrome P450, family 4, subfamily F, polypeptide 2 1.12851
BUD13 BUD13 homolog (S. cerevisiae) 1.12851
NKAIN3 Na+/K+ transporting ATPase interacting 3 1.07729
CYP4F11 cytochrome P450, family 4, subfamily F, polypeptide 11 1.01499
LOC100507144 uncharacterized LOC100507144 0.969142
BRAF B-Raf proto-oncogene, serine/threonine kinase 0.942765
P3H3 prolyl 3-hydroxylase 3 0.942765
SLC6A1 solute carrier family 6 (neurotransmitter transporter), member 1 0.899912
ZNF441 zinc finger protein 441 0.817516
ST6GALNAC5 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 0.806402
CTSH cathepsin H 0.804323
MYH11 myosin, heavy chain 11, smooth muscle 0.784165
TMBIM4 transmembrane BAX inhibitor motif containing 4 0.757258
SPARCL1 SPARC-like 1 (hevin) 0.752335
GGH gamma-glutamyl hydrolase (conjugase, folylpolygammaglutamyl hydrolase) 0.730213
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8 0.716105
CSMD1 CUB and Sushi multiple domains 1 0.710801
SLC44A3 solute carrier family 44, member 3 0.703894
PRMT8 protein arginine methyltransferase 8 0.696021
SPRED2 sprouty-related, EVH1 domain containing 2 0.684556
CHIT1 chitinase 1 (chitotriosidase) 0.675718
ALDH3B1 aldehyde dehydrogenase 3 family, member B1 0.675718