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 07/05/2024 MGI 6.24 |
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