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Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for RAI2 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID10742
Official gene symbolRAI2
Full nameretinoic acid induced 2
Aliases,-,
Gene summaryRetinoic 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. [provided by RefSeq]
LocationChromosome: X   Locus: Xp22
Gene position17879457 - 17818169  Map Viewer
Gene orientationminus
Gene size61289 bp
Gene sequence