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Symbol Name ID |
Rai1
retinoic acid induced 1 MGI:103291 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Brachycephaly |
Micrognathia |
Mandibular prognathia |
Malar flattening |
Microcephaly |
Clinodactyly of the 5th finger |
Hand polydactyly |
Toe syndactyly |
Brachydactyly |
Short palm |
Joint stiffness |
Scoliosis |
Abnormal form of the vertebral bodies |
| Disease(s) Associated with RAI1 | ||||||||||||||
| Smith-Magenis syndrome |
| Mouse Phenotypes | malocclusion |
abnormal nasal bone morphology |
broad nasal bone |
short nasal bone |
polyphalangy |
abnormal thyroid cartilage morphology |
abnormal axial skeleton morphology |
abnormal rib development |
abnormal thoracic vertebrae morphology |
kyphosis |
abnormal cervical vertebrae morphology |
fusion of atlas and odontoid process |
abnormal vertebral arch development |
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| Availability | Mouse Genotype | |||||||||||||
| Rai1tm1Jrl/Rai1tm1Jrl | ||||||||||||||
| Rai1tm1Jrl/Rai1+ | ||||||||||||||
| Rai1tm2.1Luo/Rai1tm2.1Luo Tg(Nes-cre)1Kln/? (conditional) |
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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 04/30/2024 MGI 6.23 |
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