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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	Splenomegaly
Disease(s) Associated with CPOX	Splenomegaly
hereditary coproporphyria

Mouse Phenotypes		enlarged spleen	hypochromic microcytic anemia	microcytic anemia	increased erythroblast number	abnormal erythrocyte morphology	decreased mean corpuscular hemoglobin	decreased mean corpuscular volume	increased red blood cell distribution width	anisocytosis	increased spleen red pulp amount
Availability	Mouse Genotype	enlarged spleen	hypochromic microcytic anemia	microcytic anemia	increased erythroblast number	abnormal erythrocyte morphology	decreased mean corpuscular hemoglobin	decreased mean corpuscular volume	increased red blood cell distribution width	anisocytosis	increased spleen red pulp amount
	Cpox^Rbc16/Cpox⁺
	Cpox^Rgsc0129/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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