RAI1
{{Short description|Mammalian protein found in Homo sapiens}}
{{about|the protein|the Italian television channel|Rai 1}}
{{infobox gene}}
RAI1 is a transcription factor associated with Smith–Magenis syndrome when individuals have deletions of the gene and Potocki–Lupski syndrome when individuals have a duplication. It is known as retinoic acid induced 1.
See also
External links
- [https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms GeneReviews/NIH/NCBI/UW entry on Smith-Magenis Syndrome]
- {{MeSH name|RAI1+protein,+human}}
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