Primary biliary cirrhosis Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts. (Human Disease Ontology, DOID_12236)
External Link https://www.ebi.ac.uk/gwas/search?query=Primary biliary cirrhosis
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Genes

16 genes associated with the Primary biliary cirrhosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
NAB1 NGFI-A binding protein 1 (EGR1 binding protein 1) 1.01293
TNPO3 transportin 3 0.912347
IL12A-AS1 IL12A antisense RNA 1 0.802698
TNFSF15 tumor necrosis factor (ligand) superfamily, member 15 0.793579
SPIB Spi-B transcription factor (Spi-1/PU.1 related) 0.750033
CLEC16A C-type lectin domain family 16, member A 0.686534
IL12RB2 interleukin 12 receptor, beta 2 0.661873
RAD51B RAD51 paralog B 0.637972
TIMMDC1 translocase of inner mitochondrial membrane domain containing 1 0.626595
RPS6KA4 ribosomal protein S6 kinase, 90kDa, polypeptide 4 0.572839
IKZF3 IKAROS family zinc finger 3 (Aiolos) 0.499091
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A 0.499091
PLCL2 phospholipase C-like 2 0.405958
ELMO1 engulfment and cell motility 1 0.377988
FBXL20 F-box and leucine-rich repeat protein 20 0.238523
STAT4 signal transducer and activator of transcription 4 0.220915