biliary atresia Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A cholestasis characterized by blockage of the ducts that carry bile from the liver to the gallbladder. (Human Disease Ontology, DOID_13608)
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24 genes associated with the disease biliary atresia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
WDR70 WD repeat domain 70 1.53214
LOC100506272 uncharacterized LOC100506272 1.52771
HPCAL1 hippocalcin-like 1 1.24818
LY86-AS1 LY86 antisense RNA 1 1.21954
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13 1.18117
TMEM117 transmembrane protein 117 1.14885
MAMDC2 MAM domain containing 2 1.12297
ITPK1 inositol-tetrakisphosphate 1-kinase 1.12017
LMF1 lipase maturation factor 1 1.04096
PCBP3 poly(rC) binding protein 3 1.01984
ADAMTS17 ADAM metallopeptidase with thrombospondin type 1 motif, 17 0.966942
PLEKHG1 pleckstrin homology domain containing, family G (with RhoGef domain) member 1 0.949336
VWC2L von Willebrand factor C domain containing protein 2-like 0.933664
STAM signal transducing adaptor molecule (SH3 domain and ITAM motif) 1 0.874542
NLRP5 NLR family, pyrin domain containing 5 0.859982
PSORS1C1 psoriasis susceptibility 1 candidate 1 0.831182
ADD3 adducin 3 (gamma) 0.822323
TDRD5 tudor domain containing 5 0.775452
AK8 adenylate kinase 8 0.770976
SLC39A11 solute carrier family 39, member 11 0.758762
PRKCA protein kinase C, alpha 0.726862
PRKCE protein kinase C, epsilon 0.697221
RORA RAR-related orphan receptor A 0.697221
SLCO3A1 solute carrier organic anion transporter family, member 3A1 0.687223