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Symbol
Name
ID
Proc
protein C
MGI:97771
Phenotype annotations related to nervous system
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
Availability Mouse Genotype
Proctm1Fjc/Proctm1Fjc

Contributing Projects:
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
The Jackson Laboratory