|
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 |
Large face |
Broad face |
Midface retrusion |
Broad forehead |
Prominent forehead |
Short philtrum |
Everted upper lip vermilion |
Tented upper lip vermilion |
Cleft upper lip |
Velopharyngeal insufficiency |
Cleft palate |
Open mouth |
Abnormality of the dentition |
Taurodontia |
Delayed eruption of primary teeth |
Orofacial cleft |
Anteverted nares |
Depressed nasal bridge |
Wide nasal bridge |
Short nose |
Synophrys |
Upslanted palpebral fissure |
| Disease(s) Associated with RAI1 | ||||||||||||||||||||||||||||
| Smith-Magenis syndrome |
| Mouse Phenotypes | malocclusion |
abnormal nasal bone morphology |
broad nasal bone |
short nasal bone |
abnormal snout morphology |
broad snout |
short snout |
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| Availability | Mouse Genotype | |||||||
| Rai1tm1Jrl/Rai1tm1Jrl | ||||||||
| Rai1tm1Jrl/Rai1+ | ||||||||
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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