biliary atresia Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A cholestasis characterized by blockage of the ducts that carry bile from the liver to the gallbladder. (Human Disease Ontology, DOID_13608)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0005912
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Genes

24 genes associated with the biliary atresia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
WDR70 WD repeat domain 70 1.38196
LOC100506272 uncharacterized LOC100506272 1.37637
HPCAL1 hippocalcin-like 1 1.09321
LY86-AS1 LY86 antisense RNA 1 1.06703
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13 1.03217
TMEM117 transmembrane protein 117 1.00386
MAMDC2 MAM domain containing 2 0.98241
ITPK1 inositol-tetrakisphosphate 1-kinase 0.979804
LMF1 lipase maturation factor 1 0.913571
PCBP3 poly(rC) binding protein 3 0.896026
ADAMTS17 ADAM metallopeptidase with thrombospondin type 1 motif, 17 0.851815
PLEKHG1 pleckstrin homology domain containing, family G (with RhoGef domain) member 1 0.836232
VWC2L von Willebrand factor C domain containing protein 2-like 0.82221
STAM signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 0.767696
NLRP5 NLR family, pyrin domain containing 5 0.753299
PSORS1C1 psoriasis susceptibility 1 candidate 1 0.725675
ADD3 adducin 3 (gamma) 0.717572
TDRD5 tudor domain containing 5 0.672779
AK8 adenylate kinase 8 0.668247
SLC39A11 solute carrier family 39, member 11 0.65699
PRKCA protein kinase C, alpha 0.626496
PRKCE protein kinase C, epsilon 0.598635
RORA RAR-related orphan receptor A 0.598635
SLCO3A1 solute carrier organic anion transporter family, member 3A1 0.589054