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Symbol Name ID |
Rara
retinoic acid receptor, alpha MGI:97856 |
| Darker colors indicate more annotations |
| Human Phenotypes | Bone pain |
| Disease(s) Associated with RARA | |
| acute promyelocytic leukemia |
| Mouse Phenotypes | abnormal alisphenoid bone morphology |
abnormal temporal bone squamous part morphology |
abnormal hyoid bone morphology |
abnormal incus morphology |
abnormal cricoid cartilage morphology |
abnormal thyroid cartilage morphology |
abnormal tracheal cartilage morphology |
abnormal skeleton morphology |
thoracic vertebral transformation |
abnormal cervical vertebrae morphology |
fusion of atlas and odontoid process |
abnormal cervical axis morphology |
cervical vertebral fusion |
cervical vertebral transformation |
lumbar vertebral transformation |
fusion of vertebral arches |
vertebral transformation |
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| Availability | Mouse Genotype | |||||||||||||||||
| Raratm1Ipc/Raratm1Ipc | ||||||||||||||||||
| Raratm1Ipc/Rara+ | ||||||||||||||||||
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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