PR domain containing 8, isoform CRA_a [Homo sapiens]

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PRDM8 reveals aberrant DNA methylation in aging syndromes and is relevant for hematopoietic and neuronal differentiation. [Clin Epigenetics. 2020]
PRDM8 reveals aberrant DNA methylation in aging syndromes and is relevant for hematopoietic and neuronal differentiation.
Cypris O, Eipel M, Franzen J, Rösseler C, Tharmapalan V, Kuo CC, Vieri M, Nikolić M, Kirschner M, Brümmendorf TH, et al. Clin Epigenetics. 2020 Aug 20; 12(1):125. Epub 2020 Aug 20.
PRDM8 internal promoter hyperhydroxymethylation correlates with increased expression of the corresponding transcript in Down syndrome. [Mol Med Rep. 2016]
PRDM8 internal promoter hyperhydroxymethylation correlates with increased expression of the corresponding transcript in Down syndrome.
Lu Z, Liu Y, Ren Z, Yan J. Mol Med Rep. 2016 Aug; 14(2):1227-34. Epub 2016 Jun 8.
DNA methylation in PRDM8 is indicative for dyskeratosis congenita. [Oncotarget. 2016]
DNA methylation in PRDM8 is indicative for dyskeratosis congenita.
Weidner CI, Lin Q, Birkhofer C, Gerstenmaier U, Kaifie A, Kirschner M, Bruns H, Balabanov S, Trummer A, Stockklausner C, et al. Oncotarget. 2016 Mar 8; 7(10):10765-72.

RefSeq genomic sequence
See the genomic reference sequence for the PRDM8 gene (NG_046725.1).
RefSeq protein isoforms
See 2 reference sequence protein isoforms for the PRDM8 gene.

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