Symbol Name ID |
Proc
protein C MGI:97771 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal cerebral vascular morphology |
Abnormality of the nervous system |
Cerebral palsy |
Sleep abnormality |
Headache |
Global developmental delay |
Seizure |
Disease(s) Associated with PROC | |||||||
autosomal dominant thrombophilia due to protein C deficiency | |||||||
autosomal recessive thrombophilia due to protein C deficiency | |||||||
pre-eclampsia | |||||||
protein C deficiency |
Mouse Phenotypes | 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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