|
Symbol Name ID |
Rara
retinoic acid receptor, alpha MGI:97856 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal bleeding |
Epistaxis |
Gingival bleeding |
Diffuse alveolar hemorrhage |
Oral cavity bleeding |
Bruising susceptibility |
Purpura |
Ecchymosis |
Petechiae |
Abnormal granulocytopoietic cell morphology |
Bone marrow hypercellularity |
Pancytopenia |
Anemia |
Neutropenia |
Leukocytosis |
Leukopenia |
Acute promyelocytic leukemia |
Disseminated intravascular coagulation |
Hypofibrinogenemia |
Thrombocytopenia |
| Disease(s) Associated with RARA | ||||||||||||||||||||
| acute promyelocytic leukemia |
| Mouse Phenotypes | abnormal lymphopoiesis |
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| Availability | Mouse Genotype | |
| Raratm1.1Ybe/Raratm1.1Ybe (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 05/14/2024 MGI 6.23 |
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