RAI1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
Aliases | RAI1, SMCR, SMS, retinoic acid induced 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 607642 MGI: 103291 HomoloGene: 7508 GeneCards: RAI1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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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
- GeneReviews/NIH/NCBI/UW entry on Smith-Magenis Syndrome
- RAI1+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
- 1 2 3 GRCh38: Ensembl release 89: ENSG00000108557 - Ensembl, May 2017
- 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000062115 - Ensembl, May 2017
- ↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
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