Phenotypes for Cp Heph MGI:5490776 MGI Mouse

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Phenotypes Associated with This Genotype

Allelic Composition	Cp^tm1Hrs/Cp^tm1Hrs Heph^sla/Heph^sla
Genetic Background	involves: 129X1/SvJ

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cp^tm1Hrs mutation (1 available); any Cp mutation (76 available)
Heph^sla mutation (1 available); any Heph mutation (11 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

homeostasis/metabolism

abnormal iron level ( J:196540 )

• increased iron accumulation in the retinal pigment epithelium

decreased circulating iron level ( J:196540 )

vision/eye

abnormal retina pigment epithelium morphology ( J:196540 )

• retinal pigment epithelium cells are auto-fluorescent

pigmentation

abnormal retina pigment epithelium morphology ( J:196540 )

• retinal pigment epithelium cells are auto-fluorescent

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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