RAI2, retinoic acid induced 2

RAI2, retinoic acid induced 2

• Retinoic acid plays a critical role in development, cellular growth, and differentiation. The specific function of this retinoic acid-induced gene has not yet been determined but it may play a role in development. The chromosomal location of this gene designates it to be a candidate for diseases such as Nance-Horan syndrome, sensorineural deafness, non-specific X-linked cognitive disability, oral-facial-digital syndrome, and Fried syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]

• Gene Synonyms (retinoic acid-induced protein 2,)
• NCBI Gene ID: 10742
• Species: Homo sapiens (Human)
• UNIPROT ID#>>A0A024RBZ8
  UNIPROT ID#>>B3KPD7
  UNIPROT ID#>>Q9Y5P3
  UNIPROT ID#>>B2RBE9
• 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 2 interacts with:

• adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 2
  docking protein 5
  small glutamine rich tetratricopeptide repeat containing beta
  ubiquilin 1
  ubiquilin 4

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.