RAI1
Identifiers
AliasesRAI1, SMCR, SMS, retinoic acid induced 1
External IDsOMIM: 607642 MGI: 103291 HomoloGene: 7508 GeneCards: RAI1
Orthologs
SpeciesHumanMouse
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 MbChr 11: 60.11 – 60.2 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/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.

See also


  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000108557 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000062115 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
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