abnormal hepatobiliary system development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description developmental anomaly of any of the tissues of the liver or biliary system (Mammalian Phenotype Ontology, MP_0003943)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003943
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Genes

60 gene mutations causing the abnormal hepatobiliary system development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAR adenosine deaminase, RNA-specific
ARF6 ADP-ribosylation factor 6
ARL3 ADP-ribosylation factor-like 3
B9D1 B9 protein domain 1
BMP4 bone morphogenetic protein 4
BRD1 bromodomain containing 1
CBFB core-binding factor, beta subunit
DNM1L dynamin 1-like
DPH1 diphthamide biosynthesis 1
FAM20B family with sequence similarity 20, member B
FGFR2 fibroblast growth factor receptor 2
FOXM1 forkhead box M1
GATA6 GATA binding protein 6
GIMAP1-GIMAP5 GIMAP1-GIMAP5 readthrough
GPBAR1 G protein-coupled bile acid receptor 1
HES1 hes family bHLH transcription factor 1
HHEX hematopoietically expressed homeobox
HLX H2.0-like homeobox
ICMT isoprenylcysteine carboxyl methyltransferase
JUN jun proto-oncogene
KLF6 Kruppel-like factor 6
KMT2A lysine (K)-specific methyltransferase 2A
LIG1 ligase I, DNA, ATP-dependent
MAP2K4 mitogen-activated protein kinase kinase 4
MBTD1 mbt domain containing 1
MECOM MDS1 and EVI1 complex locus
MED1 mediator complex subunit 1
MEN1 multiple endocrine neoplasia I
MET MET proto-oncogene, receptor tyrosine kinase
MKS1 Meckel syndrome, type 1
MSX1 msh homeobox 1
MYB v-myb avian myeloblastosis viral oncogene homolog
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
NCOA6 nuclear receptor coactivator 6
NF1 neurofibromin 1
NOTCH2 notch 2
NPRL3 nitrogen permease regulator-like 3 (S. cerevisiae)
ONECUT1 one cut homeobox 1
ONECUT2 one cut homeobox 2
PBX1 pre-B-cell leukemia homeobox 1
PDX1 pancreatic and duodenal homeobox 1
PEX11B peroxisomal biogenesis factor 11 beta
PKD2 polycystic kidney disease 2 (autosomal dominant)
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
PKNOX1 PBX/knotted 1 homeobox 1
PROX1 prospero homeobox 1
PTK2 protein tyrosine kinase 2
PTPN12 protein tyrosine phosphatase, non-receptor type 12
RAPGEF2 Rap guanine nucleotide exchange factor (GEF) 2
RPGRIP1L RPGRIP1-like
RXRA retinoid X receptor, alpha
SLC20A1 solute carrier family 20 (phosphate transporter), member 1
SOX17 SRY (sex determining region Y)-box 17
TCEB3 transcription elongation factor B (SIII), polypeptide 3 (110kDa, elongin A)
TGFB1 transforming growth factor, beta 1
TGFBR3 transforming growth factor, beta receptor III
TMEM67 transmembrane protein 67
UBC ubiquitin C
WT1 Wilms tumor 1
XBP1 X-box binding protein 1