|
Symbol Name ID |
Proc
protein C MGI:97771 |
| Darker colors indicate more annotations |
| Human Phenotypes | Vitreous hemorrhage |
Purpura |
Central retinal artery occlusion |
Venous insufficiency |
Abnormal cerebral vascular morphology |
Elevated diastolic blood pressure |
Elevated systolic blood pressure |
Hypertension |
Pulmonary embolism |
Abnormality of the hepatic vasculature |
Hepatosplenomegaly |
Retinal vasculitis |
| Disease(s) Associated with PROC | ||||||||||||
| antiphospholipid syndrome | ||||||||||||
| autosomal dominant thrombophilia due to protein C deficiency | ||||||||||||
| autosomal recessive thrombophilia due to protein C deficiency | ||||||||||||
| pre-eclampsia | ||||||||||||
| protein C deficiency |
| Mouse Phenotypes | bruising |
intracranial hemorrhage |
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| Availability | Mouse Genotype | ||
| Proctm1Fjc/Proctm1Fjc | |||
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 05/21/2024 MGI 6.23 |
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