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RAI1

From Wikipedia, the free encyclopedia
RAI1
Identifiers
AliasesRAI1, SMCR, SMS, retinoic acid induced 1
External IDsOMIM: 607642; MGI: 103291; HomoloGene: 7508; GeneCards: RAI1; OMA:RAI1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
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

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000108557Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000062115Ensembl, 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.