body weight changes Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group metabolic (Genetic Association Database)
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Genes

33 genes associated with the disease body weight changes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ANO3 anoctamin 3
ARFGEF1 ADP-ribosylation factor guanine nucleotide-exchange factor 1 (brefeldin A-inhibited)
BACE1 beta-site APP-cleaving enzyme 1
C4ORF26 chromosome 4 open reading frame 26
CELF6 CUGBP, Elav-like family member 6
CNTNAP5 contactin associated protein-like 5
DCC DCC netrin 1 receptor
DEFB112 defensin, beta 112
DNAH9 dynein, axonemal, heavy chain 9
FBN1 fibrillin 1
FRMD6 FERM domain containing 6
GRIA1 glutamate receptor, ionotropic, AMPA 1
ITK IL2-inducible T-cell kinase
KCNIP4 Kv channel interacting protein 4
KCNS3 potassium voltage-gated channel, modifier subfamily S, member 3
KLHL29 kelch-like family member 29
LEKR1 leucine, glutamate and lysine rich 1
MACROD2 MACRO domain containing 2
MAGI2 membrane associated guanylate kinase, WW and PDZ domain containing 2
MTMR7 myotubularin related protein 7
NRXN3 neurexin 3
PLCB1 phospholipase C, beta 1 (phosphoinositide-specific)
RBL2 retinoblastoma-like 2
RSPO2 R-spondin 2
SGCZ sarcoglycan, zeta
SLC16A7 solute carrier family 16 (monocarboxylate transporter), member 7
SLC8A1 solute carrier family 8 (sodium/calcium exchanger), member 1
STAU2 staufen double-stranded RNA binding protein 2
TMTC1 transmembrane and tetratricopeptide repeat containing 1
TTC3 tetratricopeptide repeat domain 3
UBE2E2 ubiquitin-conjugating enzyme E2E 2
VAT1L vesicle amine transport 1-like
WDR45B WD repeat domain 45B