liver fibrosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003333
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Genes

35 gene mutations causing the liver fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
AHR aryl hydrocarbon receptor
ALMS1 Alstrom syndrome protein 1
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like
CBS cystathionine-beta-synthase
CYS1 cystin 1
ENTPD1 ectonucleoside triphosphate diphosphohydrolase 1
F5 coagulation factor V (proaccelerin, labile factor)
GLMP glycosylated lysosomal membrane protein
HABP2 hyaluronan binding protein 2
HMOX1 heme oxygenase 1
IFT88 intraflagellar transport 88
IL5 interleukin 5
LDLR low density lipoprotein receptor
LTBP1 latent transforming growth factor beta binding protein 1
MC4R melanocortin 4 receptor
MIR122 microRNA 122
MKS1 Meckel syndrome, type 1
NCOA5 nuclear receptor coactivator 5
NOS2 nitric oxide synthase 2, inducible
PKD2 polycystic kidney disease 2 (autosomal dominant)
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
PLAU plasminogen activator, urokinase
PLAUR plasminogen activator, urokinase receptor
PLG plasminogen
PROC protein C (inactivator of coagulation factors Va and VIIIa)
RASSF2 Ras association (RalGDS/AF-6) domain family member 2
RELA v-rel avian reticuloendotheliosis viral oncogene homolog A
RELB v-rel avian reticuloendotheliosis viral oncogene homolog B
RPGRIP1L RPGRIP1-like
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SIRT3 sirtuin 3
TET2 tet methylcytosine dioxygenase 2
TNIP1 TNFAIP3 interacting protein 1
XYLT2 xylosyltransferase II