primary biliary cirrhosis Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts. (Human Disease Ontology, DOID_12236)
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24 genes associated with the disease primary biliary cirrhosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
NAB1 NGFI-A binding protein 1 (EGR1 binding protein 1) 1.32252
DENND1B DENN/MADD domain containing 1B 1.00628
TNFSF15 tumor necrosis factor (ligand) superfamily, member 15 0.995303
SPIB Spi-B transcription factor (Spi-1/PU.1 related) 0.945428
EXOC3L4 exocyst complex component 3-like 4 0.932337
CXCR5 chemokine (C-X-C motif) receptor 5 0.85991
CLEC16A C-type lectin domain family 16, member A 0.85991
MANBA mannosidase, beta A, lysosomal 0.850113
IL12RB2 interleukin 12 receptor, beta 2 0.825265
CAPSL calcyphosine-like 0.817078
RAD51B RAD51 paralog B 0.790827
RPS6KA4 ribosomal protein S6 kinase, 90kDa, polypeptide 4 0.69843
TNPO3 transportin 3 0.682635
RPL3 ribosomal protein L3 0.63207
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A 0.602429
IKZF3 IKAROS family zinc finger 3 (Aiolos) 0.602429
TIMMDC1 translocase of inner mitochondrial membrane domain containing 1 0.58494
POU2AF1 POU class 2 associating factor 1 0.486425
PLCL2 phospholipase C-like 2 0.486425
IL7R interleukin 7 receptor 0.449873
ELMO1 engulfment and cell motility 1 0.449873
EIF4E eukaryotic translation initiation factor 4E 0.403461
FBXL20 F-box and leucine-rich repeat protein 20 0.274608
STAT4 signal transducer and activator of transcription 4 0.256228