abnormal acute phase protein level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description deviation from the normal levels of the series of proteins found in the blood shortly after infection and which participate in the early phases of host defense against infection (Mammalian Phenotype Ontology, MP_0010211)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010211
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Genes

20 gene mutations causing the abnormal acute phase protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNTL aryl hydrocarbon receptor nuclear translocator-like
CREB3L3 cAMP responsive element binding protein 3-like 3
CRP C-reactive protein, pentraxin-related
FGA fibrinogen alpha chain
FGG fibrinogen gamma chain
GPR21 G protein-coupled receptor 21
HRG histidine-rich glycoprotein
IL1R1 interleukin 1 receptor, type I
IL1RN interleukin 1 receptor antagonist
IL6 interleukin 6
IL6R interleukin 6 receptor
LIF leukemia inhibitory factor
PLAT plasminogen activator, tissue
PLAU plasminogen activator, urokinase
PLG plasminogen
PRF1 perforin 1 (pore forming protein)
PTGER4 prostaglandin E receptor 4 (subtype EP4)
PTPN6 protein tyrosine phosphatase, non-receptor type 6
SERPINE2 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 2
TFPI tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor)