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Peptide sequence: EMLSQPNHPS GEVKAENNIE MVGESQAAKV IVSVEDAVPT IFCGKIKGLS
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 mental retardation, oral-facial-digital syndrome, and Fried syndrome. Alternate splicing results in multiple transcript variants.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Retinoic acid-induced protein 2
Gene Aliases: RAI2
UniProt ID: (Human) Q9Y5P3
Entrez Gene ID: (Human) 10742
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