nutrition disease Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An acquired metabolic disease that is characterized by an insufficient intake of food or of certain nutrients, by an inability of the body to absorb and use nutrients, or by overconsumption of certain foods. (Human Disease Ontology, DOID_374)
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Genes

49 genes involed in the disease nutrition disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ADIPOQ adiponectin, C1Q and collagen domain containing
ADRB3 adrenoceptor beta 3
AGRP agouti related neuropeptide
ALMS1 Alstrom syndrome protein 1
ARL6 ADP-ribosylation factor-like 6
BBS1 Bardet-Biedl syndrome 1
BBS10 Bardet-Biedl syndrome 10
BBS12 Bardet-Biedl syndrome 12
BBS2 Bardet-Biedl syndrome 2
BBS4 Bardet-Biedl syndrome 4
BBS5 Bardet-Biedl syndrome 5
BBS7 Bardet-Biedl syndrome 7
BBS9 Bardet-Biedl syndrome 9
CARTPT CART prepropeptide
CCDC28B coiled-coil domain containing 28B
CEP19 centrosomal protein 19kDa
CEP290 centrosomal protein 290kDa
DYRK1B dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1B
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
ENPP2 ectonucleotide pyrophosphatase/phosphodiesterase 2
FTO fat mass and obesity associated
HDAC8 histone deacetylase 8
IFT27 intraflagellar transport 27
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
KIF7 kinesin family member 7
LEP leptin
LEPR leptin receptor
LZTFL1 leucine zipper transcription factor-like 1
MC4R melanocortin 4 receptor
MKKS McKusick-Kaufman syndrome
MKS1 Meckel syndrome, type 1
MRAP2 melanocortin 2 receptor accessory protein 2
NR0B2 nuclear receptor subfamily 0, group B, member 2
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
PCSK1 proprotein convertase subtilisin/kexin type 1
PNPLA3 patatin-like phospholipase domain containing 3
POMC proopiomelanocortin
PPARG peroxisome proliferator-activated receptor gamma
RETN resistin
SLC6A14 solute carrier family 6 (amino acid transporter), member 14
TMEM67 transmembrane protein 67
TRIM32 tripartite motif containing 32
TTC21B tetratricopeptide repeat domain 21B
TTC8 tetratricopeptide repeat domain 8
TUB tubby bipartite transcription factor
UCP1 uncoupling protein 1 (mitochondrial, proton carrier)
UCP3 uncoupling protein 3 (mitochondrial, proton carrier)
VPS13B vacuolar protein sorting 13 homolog B (yeast)
WDPCP WD repeat containing planar cell polarity effector