putative Polycomb group protein ASXL2 isoform 2 [Homo sapiens]

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Diagnosis of Shashi-Pena Syndrome Caused by Chromosomal Rearrangement Using Nanopore Sequencing. [Neurol Genet. 2021]
Diagnosis of Shashi-Pena Syndrome Caused by Chromosomal Rearrangement Using Nanopore Sequencing.
Wang Y, Tan J, Wang Y, Liu A, Qiao F, Huang M, Zhang C, Zhou J, Hu P, Xu Z. Neurol Genet. 2021 Dec; 7(6):e635. Epub 2021 Nov 23.
Association between serum anti‑ASXL2 antibody levels and acute ischemic stroke, acute myocardial infarction, diabetes mellitus, chronic kidney disease and digestive organ cancer, and their possible association with atherosclerosis and hypertension. [Int J Mol Med. 2020]
Association between serum anti‑ASXL2 antibody levels and acute ischemic stroke, acute myocardial infarction, diabetes mellitus, chronic kidney disease and digestive organ cancer, and their possible association with atherosclerosis and hypertension.
Li SY, Yoshida Y, Kobayashi E, Adachi A, Hirono S, Matsutani T, Mine S, Machida T, Ohno M, Nishi E, et al. Int J Mol Med. 2020 Oct; 46(4):1274-1288. Epub 2020 Jul 29.
ASXL2 mutation is recurrent in non-de novo AML1-ETO-negative acute myeloid leukemia. [Ann Hematol. 2019]
ASXL2 mutation is recurrent in non-de novo AML1-ETO-negative acute myeloid leukemia.
Zhang X, Jin J, Yu W. Ann Hematol. 2019 Nov; 98(11):2621-2623.

RefSeq genomic sequence
See the genomic reference sequence for the ASXL2 gene (NG_052995.1).
RefSeq mRNA
See reference mRNA sequence for the ASXL2 gene (NM_001369346.1).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the ASXL2 gene.

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Protein