Bipolar disorder (body mass index interaction) Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link https://www.ebi.ac.uk/gwas/search?query=Bipolar disorder (body mass index interaction)
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Genes

21 genes associated with the Bipolar disorder (body mass index interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
LOC102724068 uncharacterized LOC102724068 0.449549
TCF7L2 transcription factor 7-like 2 (T-cell specific, HMG-box) 0.389385
TRIM42 tripartite motif containing 42 0.389385
ALOX12P2 arachidonate 12-lipoxygenase pseudogene 2 0.255654
FBXL17 F-box and leucine-rich repeat protein 17 0.165905
LOC643542 uncharacterized LOC643542 0.165905
CLHC1 clathrin heavy chain linker domain containing 1 0.165905
WWOX WW domain containing oxidoreductase 0.165905
PDZD2 PDZ domain containing 2 0.129504
TSHZ2 teashirt zinc finger homeobox 2 0.129504
ADAM19 ADAM metallopeptidase domain 19 0.129504
NAALADL2 N-acetylated alpha-linked acidic dipeptidase-like 2 0.129504
CDH23 cadherin-related 23 0.129504
RIN2 Ras and Rab interactor 2 0.129504
SLC25A36 solute carrier family 25 (pyrimidine nucleotide carrier), member 36 0.104568
TMEM132B transmembrane protein 132B 0.104568
CDH4 cadherin 4, type 1, R-cadherin (retinal) 0.085234
EFCAB10 EF-hand calcium binding domain 10 0.085234
JPH3 junctophilin 3 0.085234
PUS7 pseudouridylate synthase 7 (putative) 0.085234
FAM19A5 family with sequence similarity 19 (chemokine (C-C motif)-like), member A5 0.085234