RAI1, retinoic acid induced 1

RAI1, retinoic acid induced 1

• This gene is located within the Smith-Magenis syndrome region on chromosome 17. It is highly similar to its mouse counterpart and is expressed at high levels mainly in neuronal tissues. The protein encoded by this gene includes a polymorphic polyglutamine tract in the N-terminal domain. Expression of the mouse counterpart in neurons is induced by retinoic acid. This gene is associated with both the severity of the phenotype and the response to medication in schizophrenic patients. [provided by RefSeq, Jul 2008]

• Gene Synonyms (SMCR, SMS, retinoic acid-induced protein 1, Smith-Magenis syndrome chromosome region,)
• NCBI Gene ID: 10743
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q7Z5J4
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

retinoic acid induced 1 interacts with:

• chromobox 1
  DNA topoisomerase II binding protein 1
  HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2
  mastermind like transcriptional coactivator 3
  metastasis associated 1
  mitogen-activated protein kinase 8 interacting protein 2
  N-acetylglucosamine kinase
  ring finger protein 123
  sirtuin 7
  tescalcin
  vir like m6A methyltransferase associated
  zinc finger protein 496

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.