RAI1
Identifiers
Aliases	RAI1, SMCR, SMS, retinoic acid induced 1
External IDs	OMIM: 607642; MGI: 103291; HomoloGene: 7508; GeneCards: RAI1; OMA:RAI1 - orthologs
Gene location (Human) Chr. Chromosome 17 (human)[1] Band 17p11.2 Start 17,681,458 bp[1] End 17,811,453 bp[1]
Gene location (Mouse) Chr. Chromosome 11 (mouse)[2] Band 11|11 B1.3-B2 Start 60,105,013 bp[2] End 60,199,197 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in Top expressed in More reference expression data BioGPS n/a
Gene ontology Molecular function Cellular component Biological process Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 10743 19377 Ensembl ENSG00000108557 ENSMUSG00000062115 UniProt Q7Z5J4 Q61818 RefSeq (mRNA) NM_030665 NM_017574 NM_152256 NM_001037764 NM_009021 RefSeq (protein) NP_109590 NP_001032853 NP_033047 Location (UCSC) Chr 17: 17.68 – 17.81 Mb Chr 11: 60.11 – 60.2 Mb PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

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

• GeneReviews/NIH/NCBI/UW entry on Smith-Magenis Syndrome
• RAI1+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)