liver hemorrhage Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description bleeding within the liver (Mammalian Phenotype Ontology, MP_0003888)
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28 gene mutations causing the liver hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
ADM adrenomedullin
CCR2 chemokine (C-C motif) receptor 2
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CXCL12 chemokine (C-X-C motif) ligand 12
FAIM Fas apoptotic inhibitory molecule
FES FES proto-oncogene, tyrosine kinase
FGA fibrinogen alpha chain
FKBP1A FK506 binding protein 1A, 12kDa
GYS1 glycogen synthase 1 (muscle)
IKBKB inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase beta
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
KRT8 keratin 8, type II
LIF leukemia inhibitory factor
LMF1 lipase maturation factor 1
MAP2K4 mitogen-activated protein kinase kinase 4
MKL2 MKL/myocardin-like 2
NF1 neurofibromin 1
PILRA paired immunoglobin-like type 2 receptor alpha
PRDX6 peroxiredoxin 6
PTK2 protein tyrosine kinase 2
RAMP2 receptor (G protein-coupled) activity modifying protein 2
RB1CC1 RB1-inducible coiled-coil 1
TAB2 TGF-beta activated kinase 1/MAP3K7 binding protein 2
TBK1 TANK-binding kinase 1
TDG thymine-DNA glycosylase
TLL1 tolloid-like 1
TNNT3 troponin T type 3 (skeletal, fast)