RAI2

RAI2
Identifiers
Aliases	RAI2, retinoic acid induced 2
External IDs	OMIM: 300217; MGI: 1344378; HomoloGene: 11034; GeneCards: RAI2; OMA:RAI2 - orthologs
Gene location (Human)
Chr.	X chromosome (human)
End	17,861,337 bp
Gene location (Mouse)
Chr.	X chromosome (mouse)
End	160,562,492 bp
RNA expression pattern
	Top expressed in
	left uterine tube; ; urethra; ; right lung; ; canal of the cervix; ; body of uterus; ; saphenous vein; ; gastric mucosa; ; left ovary; ; vena cava; ; decidua;
	Top expressed in
	myocardium of ventricle; ; intercostal muscle; ; cumulus cell; ; supraoptic nucleus; ; pineal gland; ; aortic valve; ; muscle of thigh; ; islet of Langerhans; ; Rostral migratory stream; ; ganglionic eminence;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	protein binding; molecular function;
Cellular component	cellular component;
Biological process	embryo development ending in birth or egg hatching;
	Sources:Amigo / QuickGO
Orthologs
	10742
	24004
	ENSG00000131831
	ENSMUSG00000043518
	Q9Y5P3
	Q9QVY8
	NM_001172732; NM_001172739; NM_001172743; NM_021785
	NM_001103367; NM_198409
NP_001166203; NP_001166210; NP_001166214; NP_068557; NP_001166210.1;
	NP_001166214.1; NP_068557.3
	NP_001096837; NP_940801
	Wikidata
View/Edit Human	View/Edit Mouse

Retinoic acid-induced protein 2 is a protein that in humans is encoded by the RAI2 gene.^[5]^[6]^[7]

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.^[7]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000131831 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000043518 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Walpole SM, Hiriyana KT, Nicolaou A, Bingham EL, Durham J, Vaudin M, Ross MT, Yates JR, Sieving PA, Trump D (May 1999). "Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22". Genomics. 55 (3): 275–83. doi:10.1006/geno.1998.5667. PMID 10049581.
^ Walpole SM, Ronce N, Grayson C, Dessay B, Yates JR, Trump D, Toutain A (Jul 1999). "Exclusion of RAI2 as the causative gene for Nance-Horan syndrome". Hum Genet. 104 (5): 410–1. doi:10.1007/s004390050976. PMID 10394933. S2CID 5675053.
^ ^a ^b "Entrez Gene: RAI2 retinoic acid induced 2".

Lim J, Hao T, Shaw C, et al. (2006). "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration". Cell. 125 (4): 801–14. doi:10.1016/j.cell.2006.03.032. PMID 16713569.
Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.

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