Malnutrition Gene Set

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

27 genes associated with the Malnutrition phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
AHSG alpha-2-HS-glycoprotein
APOE apolipoprotein E
CAT catalase
CBS cystathionine-beta-synthase
CDKAL1 CDK5 regulatory subunit associated protein 1-like 1
CDKN2A cyclin-dependent kinase inhibitor 2A
CDKN2B cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4)
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9
CYP2E1 cytochrome P450, family 2, subfamily E, polypeptide 1
DRD2 dopamine receptor D2
DRD4 dopamine receptor D4
GPX1 glutathione peroxidase 1
HHEX hematopoietically expressed homeobox
IGF2BP2 insulin-like growth factor 2 mRNA binding protein 2
IL10 interleukin 10
IL6 interleukin 6
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
PAX6 paired box 6
SIRT1 sirtuin 1
SLC30A8 solute carrier family 30 (zinc transporter), member 8
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
SOD2 superoxide dismutase 2, mitochondrial
TCF7L2 transcription factor 7-like 2 (T-cell specific, HMG-box)
TNF tumor necrosis factor