RecName: Full=Arginine-glutamic acid dipeptide repeats protein; AltNam - Protein

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Genotype-phenotype correlations in individuals with pathogenic RERE variants. [Hum Mutat. 2018]
Genotype-phenotype correlations in individuals with pathogenic RERE variants.
Jordan VK, Fregeau B, Ge X, Giordano J, Wapner RJ, Balci TB, Carter MT, Bernat JA, Moccia AN, Srivastava A, et al. Hum Mutat. 2018 May; 39(5):666-675. Epub 2018 Jan 25.
RERE deficiency contributes to the development of orofacial clefts in humans and mice. [Hum Mol Genet. 2021]
RERE deficiency contributes to the development of orofacial clefts in humans and mice.
Kim BJ, Zaveri HP, Kundert PN, Jordan VK, Scott TM, Carmichael J, Scott DA. Hum Mol Genet. 2021 May 12; 30(7):595-602.
RERE deficiency causes retinal and optic nerve atrophy through degeneration of retinal cells. [Dev Dyn. 2021]
RERE deficiency causes retinal and optic nerve atrophy through degeneration of retinal cells.
Kim BJ, Scott DA. Dev Dyn. 2021 Oct; 250(10):1398-1409. Epub 2021 Mar 29.

RefSeq protein isoforms
See 10 reference sequence protein isoforms for the Rere gene.

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Transcript/Protein Information [PANTHER Classification System]
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PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein