RecName: Full=Condensin-2 complex subunit G2; AltName: Full=Chromosome - Protein

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Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies. [Am J Hum Genet. 2019]
Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies.
Khan TN, Khan K, Sadeghpour A, Reynolds H, Perilla Y, McDonald MT, Gallentine WB, Baig SM, Task Force for Neonatal Genomics, Davis EE, et al. Am J Hum Genet. 2019 Jan 3; 104(1):94-111.
Dhx38 is required for the maintenance and differentiation of erythro-myeloid progenitors and hematopoietic stem cells by alternative splicing. [Development. 2022]
Dhx38 is required for the maintenance and differentiation of erythro-myeloid progenitors and hematopoietic stem cells by alternative splicing.
Tu J, Yu S, Li J, Ren M, Zhang Y, Luo J, Sun K, Lv Y, Han Y, Huang Y, et al. Development. 2022 Sep 1; 149(17). Epub 2022 Aug 30.
A gene expression screen in zebrafish embryogenesis. [Genome Res. 2001]
A gene expression screen in zebrafish embryogenesis.
Kudoh T, Tsang M, Hukriede NA, Chen X, Dedekian M, Clarke CJ, Kiang A, Schultz S, Epstein JA, Toyama R, et al. Genome Res. 2001 Dec; 11(12):1979-87.

RefSeq protein isoforms
See 2 reference sequence protein isoforms for the ncapg2 gene.

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