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Phenotypes Associated with This Genotype
Genotype
MGI:5488915
Allelic
Composition
Cpoxnct/Cpoxnct
Genetic
Background
involves: BALB/cCrSlc
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cpoxnct mutation (1 available); any Cpox mutation (9 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• at 10 weeks
• however, mice also expression a transgene containing the endogenous gene do not develop cataracts during the 6 month observation period

Mouse Models of Human Disease
OMIM ID Ref(s)
Coproporphyria, Hereditary; HCP 121300 J:196645


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
11/29/2016
MGI 6.06
The Jackson Laboratory