abnormal circulating fibrinogen level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description deviation from the normal levels in the blood of a globulin that is converted into fibrin by the action of thrombin in the presence of ionized calcium to produce coagulation of the blood (Mammalian Phenotype Ontology, MP_0010213)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010213
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Genes

6 gene mutations causing the abnormal circulating fibrinogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNTL aryl hydrocarbon receptor nuclear translocator-like
FGA fibrinogen alpha chain
FGG fibrinogen gamma chain
HRG histidine-rich glycoprotein
PLG plasminogen
PRF1 perforin 1 (pore forming protein)