WD repeat domain 26, isoform CRA_c [Homo sapiens]

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Skraban-Deardorff intellectual disability syndrome-associated mutations in WDR26 impair CTLH E3 complex assembly. [FEBS Lett. 2024]
Skraban-Deardorff intellectual disability syndrome-associated mutations in WDR26 impair CTLH E3 complex assembly.
Gross A, Müller J, Chrustowicz J, Strasser A, Gottemukkala KV, Sherpa D, Schulman BA, Murray PJ, Alpi AF. FEBS Lett. 2024 May; 598(9):978-994. Epub 2024 Apr 4.
Two Novel Variants of WDR26 in Chinese Patients with Intellectual Disability. [Genes (Basel). 2022]
Two Novel Variants of WDR26 in Chinese Patients with Intellectual Disability.
Hu J, Xu M, Zhu X, Zhang Y. Genes (Basel). 2022 May 2; 13(5). Epub 2022 May 2.
Detection of Disease-Causing SNVs/Indels and CNVs in Single Test Based on Whole Exome Sequencing: A Retrospective Case Study in Epileptic Encephalopathies. [Front Pediatr. 2021]
Detection of Disease-Causing SNVs/Indels and CNVs in Single Test Based on Whole Exome Sequencing: A Retrospective Case Study in Epileptic Encephalopathies.
Sun D, Liu Y, Cai W, Ma J, Ni K, Chen M, Wang C, Liu Y, Zhu Y, Liu Z, et al. Front Pediatr. 2021; 9:635703. Epub 2021 May 13.

RefSeq genomic sequence
See the genomic reference sequence for the WDR26 gene (NG_047198.1).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the WDR26 gene.

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