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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 (18 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
DO ID OMIM ID(s) Ref(s)
hereditary coproporphyria DOID:13269 OMIM:121300
J:196645


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
02/04/2020
MGI 6.14
The Jackson Laboratory