Symbol Name ID |
Rai1
retinoic acid induced 1 MGI:103291 |
Darker colors indicate more annotations |
Human Phenotypes | Delayed puberty |
Short stature |
Failure to thrive in infancy |
Increased body weight |
Obesity |
Disease(s) Associated with RAI1 | |||||
Smith-Magenis syndrome |
Mouse Phenotypes | increased body fat mass |
malocclusion |
abnormal nasal bone morphology |
broad nasal bone |
short nasal bone |
abnormal snout morphology |
broad snout |
short snout |
increased lean body mass |
decreased body weight |
increased body weight |
obese |
decreased body size |
postnatal growth retardation |
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Availability | Mouse Genotype | ||||||||||||||
Rai1tm1Jrl/Rai1tm1Jrl | |||||||||||||||
Rai1tm1Jrl/Rai1+ | |||||||||||||||
Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-Rai1,-EGFP)463Walz/0 |
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Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-Rai1,-EGFP)479Walz/0 |
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Rai1tm2.1Luo/Rai1tm2.1Luo Tg(Nes-cre)1Kln/? (conditional) |
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Rai1tm2.1Luo/Rai1tm2.1Luo Slc17a6tm2(cre)Lowl/? (conditional) |
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Rai1tm2.1Luo/Rai1tm2.1Luo Tg(Sim1-cre)1Lowl/? (conditional) |
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Rai1tm2.1Luo/Rai1tm2.1Luo Tg(Nr5a1-cre)7Lowl/? (conditional) |
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Rai1tm2.1Luo/Rai1+ Tg(Nes-cre)1Kln/? (conditional) |
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Rai1tm2.1Luo/Rai1+ Slc17a6tm2(cre)Lowl/? (conditional) |
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Rai1tm2.1Luo/Rai1+ Tg(Sim1-cre)1Lowl/? (conditional) |
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Rai1tm2.1Luo/Rai1+ Tg(Nr5a1-cre)7Lowl/? (conditional) |
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Rai1tm2.2Luo/Rai1tm2.1Luo Tg(Nes-cre)1Kln/? (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 04/30/2024 MGI 6.23 |
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