weight loss Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Reduction inexisting body weight. (Human Phenotype Ontology, HP_0001824)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0001824
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26 genes associated with the weight loss phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive) 1.1784
ZBED8 zinc finger, BED-type containing 8 1.09906
CLNS1A chloride channel, nucleotide-sensitive, 1A 1.00352
SYNPO2 synaptopodin 2 0.767696
GUCY1A2 guanylate cyclase 1, soluble, alpha 2 0.672779
CLASP1 cytoplasmic linker associated protein 1 0.630903
FAM198A family with sequence similarity 198, member A 0.630262
AAMDC adipogenesis associated, Mth938 domain containing 0.616892
KCNQ5 potassium channel, voltage gated KQT-like subfamily Q, member 5 0.576102
KRT81 keratin 81, type II 0.568635
COL4A3BP collagen, type IV, alpha 3 (Goodpasture antigen) binding protein 0.550969
BIK BCL2-interacting killer (apoptosis-inducing) 0.531556
TCOF1 Treacher Collins-Franceschetti syndrome 1 0.528162
HSD17B3 hydroxysteroid (17-beta) dehydrogenase 3 0.528162
OPALIN oligodendrocytic myelin paranodal and inner loop protein 0.522995
ANKRD31 ankyrin repeat domain 31 0.50668
LVRN laeverin 0.486856
IGF1R insulin-like growth factor 1 receptor 0.481287
RAI14 retinoic acid induced 14 0.472241
TTF2 transcription termination factor, RNA polymerase II 0.470822
CLN6 ceroid-lipofuscinosis, neuronal 6, late infantile, variant 0.466305
HOXA-AS3 HOXA cluster antisense RNA 3 0.461231
TBC1D14 TBC1 domain family, member 14 0.458078
SLCO6A1 solute carrier organic anion transporter family, member 6A1 0.453371
CKAP2 cytoskeleton associated protein 2 0.436592
CLHC1 clathrin heavy chain linker domain containing 1 0.42535