Nutrition Disorders Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

6 genes associated with the Nutrition Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
APOE apolipoprotein E
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CYP3A7 cytochrome P450, family 3, subfamily A, polypeptide 7
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor