abnormal gallbladder physiology Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A functional anomaly of the gallbladder. (Human Phenotype Ontology, HP_0012438)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0012438
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Genes

7 genes associated with the abnormal gallbladder physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
DPP4 dipeptidyl-peptidase 4 1.86621
LINC01549 long intergenic non-protein coding RNA 1549 1.83145
NTM neurotrimin 1.76636
ANKRD44 ankyrin repeat domain 44 1.74402
HS6ST3 heparan sulfate 6-O-sulfotransferase 3 1.68057
PTPRT protein tyrosine phosphatase, receptor type, T 0.802966
FXR1 fragile X mental retardation, autosomal homolog 1 0.597345