|
Symbol Name ID |
Rai1
retinoic acid induced 1 MGI:103291 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of the thyroid gland |
Hypothyroidism |
Delayed puberty |
Precocious puberty |
| Disease(s) Associated with RAI1 | ||||
| Smith-Magenis syndrome |
| Mouse Phenotypes | increased amylin secretion |
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| Availability | Mouse Genotype | |
| 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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