Symbol Name ID |
Hjv
hemojuvelin BMP co-receptor MGI:1916835 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal bleeding |
Splenomegaly |
Disease(s) Associated with HJV | ||
hemochromatosis | ||
hemochromatosis type 2A |
Mouse Phenotypes | hematopoietic system phenotype |
increased hemoglobin content |
increased mean corpuscular hemoglobin |
abnormal macrophage morphology |
decreased spleen iron level |
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Availability | Mouse Genotype | |||||
Hjvtm1Arbr/Hjvtm1Arbr | ||||||
Hjvtm1b(KOMP)Wtsi/Hjvtm1b(KOMP)Wtsi | ||||||
Hjvtm1Nca/Hjvtm1Nca | * | |||||
Hjvtm1Kpan/Hjvtm1Kpan Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ (conditional) |
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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