RAI2

RAI2
Identifiers
Aliases	RAI2, retinoic acid induced 2
External IDs	MGI: 1344378 HomoloGene: 11034 GeneCards: RAI2
Gene ontology Molecular function • protein binding Cellular component • cellular component Biological process • embryo development Sources:Amigo / QuickGO
RNA expression pattern
More reference expression data
Orthologs
Species	Human	Mouse
Entrez	10742	24004
Ensembl	ENSG00000131831	ENSMUSG00000043518
UniProt	Q9Y5P3	Q9QVY8
RefSeq (mRNA)	NM_001172732 NM_001172739 NM_001172743 NM_021785	NM_001103367 NM_198409
RefSeq (protein)	NP_001166203 NP_001166210 NP_001166214 NP_068557 NP_001166210.1 NP_001166214.1 NP_068557.3	NP_001096837 NP_940801
Location (UCSC)	Chr X: 17.8 – 17.86 Mb	Chr X: 161.72 – 161.78 Mb
PubMed search

10742

24004

ENSG00000131831

ENSMUSG00000043518

Q9Y5P3

Q9QVY8

NM_001172732
NM_001172739
NM_001172743
NM_021785

NM_001103367
NM_198409

NP_001166214.1
NP_068557.3

NP_001096837
NP_940801

Retinoic acid-induced protein 2 is a protein that in humans is encoded by the RAI2 gene.

Retinoic acid plays a critical role in development, cellular growth, and differentiation. The specific function of this intronless, retinoic acid-induced gene has not yet been determined; however, it has been suggested to play a role in development. Localization 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.

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Wikipedia