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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)
- ^ a b c GRCh38: Ensembl release 89: ENSG00000108557 – Ensembl, May 2017
- ^ a b c 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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