RAI2: Difference between revisions
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'''Retinoic acid-induced protein 2''' is a [[protein]] that in humans is encoded by the ''RAI2'' [[gene]].<ref name="pmid10049581">{{cite journal | vauthors = Walpole SM, Hiriyana KT, Nicolaou A, Bingham EL, Durham J, Vaudin M, Ross MT, Yates JR, Sieving PA, Trump D | title = Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22 | journal = Genomics | volume = 55 | issue = 3 | pages = 275–83 |date=May 1999 | pmid = 10049581 | pmc = | doi = 10.1006/geno.1998.5667 }}</ref><ref name="pmid10394933">{{cite journal | vauthors = Walpole SM, Ronce N, Grayson C, Dessay B, Yates JR, Trump D, Toutain A | title = Exclusion of RAI2 as the causative gene for Nance-Horan syndrome | journal = Hum Genet | volume = 104 | issue = 5 | pages = 410–1 |date=Jul 1999 | pmid = 10394933 | pmc = | doi =10.1007/s004390050976 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: RAI2 retinoic acid induced 2| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10742| accessdate = }}</ref> | '''Retinoic acid-induced protein 2''' is a [[protein]] that in humans is encoded by the ''RAI2'' [[gene]].<ref name="pmid10049581">{{cite journal | vauthors = Walpole SM, Hiriyana KT, Nicolaou A, Bingham EL, Durham J, Vaudin M, Ross MT, Yates JR, Sieving PA, Trump D | title = Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22 | journal = Genomics | volume = 55 | issue = 3 | pages = 275–83 |date=May 1999 | pmid = 10049581 | pmc = | doi = 10.1006/geno.1998.5667 }}</ref><ref name="pmid10394933">{{cite journal | vauthors = Walpole SM, Ronce N, Grayson C, Dessay B, Yates JR, Trump D, Toutain A | title = Exclusion of RAI2 as the causative gene for Nance-Horan syndrome | journal = Hum Genet | volume = 104 | issue = 5 | pages = 410–1 |date=Jul 1999 | pmid = 10394933 | pmc = | doi =10.1007/s004390050976 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: RAI2 retinoic acid induced 2| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10742| accessdate = }}</ref> | ||
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| summary_text = 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.<ref name="entrez" /> | | summary_text = [[Retinoic acid]] plays a critical role in development, [[cellular growth]], and [[cell differentiation|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]].<ref name="entrez" /> | ||
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Latest revision as of 14:48, 20 February 2018
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Retinoic acid-induced protein 2 is a protein that in humans is encoded by the RAI2 gene.[1][2][3]
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.[3]
References
- ↑ 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.
- ↑ 3.0 3.1 "Entrez Gene: RAI2 retinoic acid induced 2".
Further reading
- 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. doi:10.1038/nature04209. PMID 16189514.
- 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. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
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