RAI2

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]

Description

Retinoic acid induced 2

Tissue specificity

Low tissue specificity

Subcell location

Plasma membrane

Predicted location

Intracellular

Protein family

Mapped to neXtProt
Mapped to UniProt SWISS-PROT
Predicted intracellular proteins

Chromosome

X (17800049 - 17861337)

Ensembl ID

ENSG00000131831  (ver. 103.38)

Orthologs

Mouse Rai2: ENSMUSG00000043518

UniProt

Q9Y5P3

neXtProt

NX_Q9Y5P3

Human splice variants
Mouse splice variants

Protein structure