vitamin metabolic disorder Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description An inherited metabolic disorder resulting from a deficiency in vitamin or vitamin cofactor transport or metabolism. (Human Disease Ontology, DOID_0050718)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:0050718
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Genes

14 genes associated with the disease vitamin metabolic disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
GC group-specific component (vitamin D binding protein) 3.11182
NADSYN1 NAD synthetase 1 2.20601
CYP2R1 cytochrome P450, family 2, subfamily R, polypeptide 1 2.01212
FUT2 fucosyltransferase 2 (secretor status included) 1.94711
FFAR4 free fatty acid receptor 4 1.79589
CYP4F2 cytochrome P450, family 4, subfamily F, polypeptide 2 1.57556
DAB1 Dab, reelin signal transducer, homolog 1 (Drosophila) 1.44383
SCARB1 scavenger receptor class B, member 1 1.43537
MS4A3 membrane-spanning 4-domains, subfamily A, member 3 (hematopoietic cell-specific) 1.34295
FUT6 fucosyltransferase 6 (alpha (1,3) fucosyltransferase) 1.22685
RBFOX1 RNA binding protein, fox-1 homolog (C. elegans) 1 0.99494
KMT2C lysine (K)-specific methyltransferase 2C 0.988032
CLYBL citrate lyase beta like 0.831584
ADGRG5 adhesion G protein-coupled receptor G5 0.819144