biliary dyskinesia Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A gallbladder disease characterized by altered tonus of the sphincter of Oddi, disturbance in the coordination of contraction of the biliary ducts, and/or reduction in the speed of emptying of the biliary tree. (Human Disease Ontology, DOID_4140)
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Genes

22 genes co-occuring with the disease biliary dyskinesia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
CCK cholecystokinin 2.5082
ECRP ribonuclease, RNase A family, 2 (liver, eosinophil-derived neurotoxin) pseudogene 1.59653
SOBP sine oculis binding protein homolog (Drosophila) 1.58939
STK10 serine/threonine kinase 10 0.900746
CCBL1 cysteine conjugate-beta lyase, cytoplasmic 0.840525
HOPX HOP homeobox 0.774932
ALPPL2 alkaline phosphatase, placental-like 2 0.51919
ALPP alkaline phosphatase, placental 0.518805
ALPL alkaline phosphatase, liver/bone/kidney 0.51842
EFS embryonal Fyn-associated substrate 0.505739
TES testin LIM domain protein 0.399707
MLN motilin 0.349349
GH1 growth hormone 1 0.339806
F10 coagulation factor X 0.329565
LCT lactase 0.300533
IRF6 interferon regulatory factor 6 0.285086
UGT1A6 UDP glucuronosyltransferase 1 family, polypeptide A6 0.266558
C6ORF25 chromosome 6 open reading frame 25 0.264077
IDH2 isocitrate dehydrogenase 2 (NADP+), mitochondrial 0.23353
ALOX5 arachidonate 5-lipoxygenase 0.204593
IDH1 isocitrate dehydrogenase 1 (NADP+), soluble 0.198709
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1 0.194548