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Symbol
Name
ID
Cpox
coproporphyrinogen oxidase
MGI:104841
Phenotype annotations related to hematopoietic system
Darker colors indicate more annotations
Human Phenotypes
Congenital hemolytic anemia
Splenomegaly
Disease(s) Associated with CPOX
hereditary coproporphyria

Mouse Phenotypes
hypochromic microcytic anemia
microcytic anemia
increased erythroblast number
abnormal erythrocyte morphology
decreased mean corpuscular volume
increased red blood cell distribution width
increased spleen red pulp amount
enlarged spleen
Availability Mouse Genotype
CpoxRbc16/Cpox+

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
11/12/2019
MGI 6.14
The Jackson Laboratory