Symbol Name ID |
Cp
ceruloplasmin MGI:88476 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Anemia |
Disease(s) Associated with CP | |
aceruloplasminemia |
Mouse Phenotypes | hematopoietic system phenotype |
abnormal Kupffer cell morphology |
microcytic anemia |
decreased hemoglobin content |
decreased mean corpuscular hemoglobin |
decreased mean corpuscular hemoglobin concentration |
decreased mean corpuscular volume |
increased spleen iron level |
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Availability | Mouse Genotype | ||||||||
Cptm1b(KOMP)Wtsi/Cptm1b(KOMP)Wtsi | |||||||||
Cptm1Hrs/Cptm1Hrs | * | ||||||||
Cptm1Yos/Cptm1Yos |
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 04/23/2024 MGI 6.23 |
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