abnormal biliary tract physiology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A functional abnormality of the biliary tree. (Human Phenotype Ontology, HP_0012439)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012439
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Genes

9 genes associated with the abnormal biliary tract physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4
MKS1 Meckel syndrome, type 1
NPHP3 nephronophthisis 3 (adolescent)
PHKG2 phosphorylase kinase, gamma 2 (testis)
POLG polymerase (DNA directed), gamma
RPGRIP1L RPGRIP1-like
TMEM216 transmembrane protein 216
TMEM67 transmembrane protein 67
Funding