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Phenotypes Associated with This Genotype
Genotype
MGI:2687183
Allelic
Composition
Hfetm2Nca/Hfetm2Nca
Urodtm1Kush/Urod+
Genetic
Background
involves: C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hfetm2Nca mutation (1 available); any Hfe mutation (35 available)
Urodtm1Kush mutation (0 available); any Urod mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• increased urinary porphyrin concentration (hepatic levels were also increased)

liver/biliary system

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
porphyria cutanea tarda DOID:3132 OMIM:176090
OMIM:176100
J:66704


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
11/19/2024
MGI 6.24
The Jackson Laboratory