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 |
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 |
|
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 03/25/2025 MGI 6.24 |
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