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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cpox
coproporphyrinogen oxidase
MGI:104841
19 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cpoxnct/Cpoxnct
involves: BALB/cCrSlc
cataract J:196645
Cpoxnct/Cpoxnct
Not Specified
abnormal lens fiber morphology J:5481
abnormal lens morphology J:5481, J:6014
cataract J:5481
hydropic eye lens fibers J:5481
CpoxRbc16/Cpox+
involves: C57BL/6
abnormal erythrocyte morphology J:244493
decreased mean corpuscular volume J:244493
enlarged spleen J:244493
hypochromic microcytic anemia J:244493
increased circulating ferritin level J:244493
increased erythroblast number J:244493
increased red blood cell distribution width J:244493
increased spleen red pulp amount J:244493
microcytic anemia J:244493
porphyria J:244493
CpoxRbc16/CpoxRbc16
involves: C57BL/6
abnormal pharyngeal arch morphology J:244493
absent forelimb buds J:244493
embryonic growth retardation J:244493
embryonic lethality during organogenesis, complete penetrance J:244493
open neural tube J:244493

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/31/2018
MGI 6.12
The Jackson Laboratory