RAI2 retinoic acid induced 2 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 10742)
Source: NCBI Gene (ID 10742)
Symbol: RAI2
Full name: retinoic acid induced 2
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Summary: 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]
Expression: Ubiquitous expression in endometrium (RPKM 19.5), ovary (RPKM 15.2) and 23 other tissues
Orthologs: mouse
Gene size: 61250bp
Exon count: 5