Symbol Name ID |
Fga
fibrinogen alpha chain MGI:1316726 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal bleeding |
Abnormal umbilical stump bleeding |
Epistaxis |
Gingival bleeding |
Gastrointestinal hemorrhage |
Hematemesis |
Epidural hemorrhage |
Subdural hemorrhage |
Persistent bleeding after trauma |
Prolonged bleeding after dental extraction |
Prolonged bleeding following circumcision |
Bruising susceptibility |
Purpura |
Petechiae |
Anemia |
Afibrinogenemia |
Hypofibrinogenemia |
Elevated erythrocyte sedimentation rate |
Splenic rupture |
Splenomegaly |
Hepatosplenomegaly |
Disease(s) Associated with FGA | |||||||||||||||||||||
congenital afibrinogenemia | |||||||||||||||||||||
familial visceral amyloidosis |
Mouse Phenotypes | decreased platelet aggregation |
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Availability | Mouse Genotype | |
Fgatm1Jld/Fgatm1Jld |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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