dnaJ homolog subfamily C member 21 isoform X2 [Homo sapiens]

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Refining the phenotype associated with biallelic DNAJC21 mutations. [Clin Genet. 2018]
Refining the phenotype associated with biallelic DNAJC21 mutations.
D'Amours G, Lopes F, Gauthier J, Saillour V, Nassif C, Wynn R, Alos N, Leblanc T, Capri Y, Nizard S, et al. Clin Genet. 2018 Aug; 94(2):252-258. Epub 2018 Jun 7.
Molecular basis of the human ribosomopathy Shwachman-Diamond syndrome. [Adv Biol Regul. 2018]
Molecular basis of the human ribosomopathy Shwachman-Diamond syndrome.
Warren AJ. Adv Biol Regul. 2018 Jan; 67:109-127. Epub 2017 Sep 6.
Biallelic mutations in DNAJC21 cause Shwachman-Diamond syndrome. [Blood. 2017]
Biallelic mutations in DNAJC21 cause Shwachman-Diamond syndrome.
Dhanraj S, Matveev A, Li H, Lauhasurayotin S, Jardine L, Cada M, Zlateska B, Tailor CS, Zhou J, Mendoza-Londono R, et al. Blood. 2017 Mar 16; 129(11):1557-1562. Epub 2017 Jan 6.

RefSeq genomic sequence
See the genomic reference sequence for the DNAJC21 gene (NG_052822.1).
RefSeq mRNA
See reference mRNA sequence for the DNAJC21 gene (XM_011513966.3).
RefSeq protein isoforms
See 15 reference sequence protein isoforms for the DNAJC21 gene.

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Protein