RAI1
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.
| retinoic acid induced 1 | |
|---|---|
| Identifiers | |
| Symbol | RAI1 |
| NCBI gene | 10743 |
| HGNC | 9834 |
| OMIM | 607642 |
| RefSeq | NM_030665 |
| UniProt | Q7Z5J4 |
| Other data | |
| Locus | Chr. 17 p11.2 |
External links
- GeneReviews/NIH/NCBI/UW entry on Smith-Magenis Syndrome
- RAI1+protein,+human at the US National Library of Medicine Medical Subject Headings (MeSH)
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