RAI1
| 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 | ||||||
| |||||||
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.
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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Categories:
- Genes on human chromosome 17
- Biochemistry stubs