Symbol Name ID |
Trf
transferrin MGI:98821 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Anemia |
Hypochromic anemia |
Disease(s) Associated with TF | ||
atransferrinemia |
Mouse Phenotypes | hematopoietic system phenotype |
hypochromic anemia |
decreased erythrocyte cell number |
decreased hematocrit |
decreased hemoglobin content |
abnormal mean corpuscular hemoglobin |
increased mean corpuscular hemoglobin |
decreased mean corpuscular hemoglobin concentration |
decreased mean corpuscular volume |
increased mean corpuscular volume |
anisocytosis |
poikilocytosis |
spherocytosis |
abnormal reticulocyte morphology |
|
Availability | Mouse Genotype | ||||||||||||||
Trfhpx/Trfhpx | |||||||||||||||
Trfem1(IMPC)J/Trf+ | |||||||||||||||
Trfem1(IMPC)Rbrc/Trf+ | |||||||||||||||
Trfhpx/Trf+ | * |
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 07/05/2024 MGI 6.24 |
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