Homo sapiens ABL proto-oncogene 1, non-receptor tyrosine kinase (ABL1) - Nucleotide

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Validation of a novel NGS based BCR::ABL1 kinase domain mutation detection assay in Indian cohort. [Sci Rep. 2024]
Validation of a novel NGS based BCR::ABL1 kinase domain mutation detection assay in Indian cohort.
Chaudhary P, Chaudhary S, Patel F, Patel S, Vaishnani T, Trivedi N, Patel D, Sonagara T, Hirapara A, Vyas K, et al. Sci Rep. 2024 Jul 8; 14(1):15745. Epub 2024 Jul 8.
Human ABL1 deficiency syndrome (HADS) is a recognizable syndrome distinct from ABL1-related congenital heart defects and skeletal malformations syndrome. [Hum Genet. 2024]
Human ABL1 deficiency syndrome (HADS) is a recognizable syndrome distinct from ABL1-related congenital heart defects and skeletal malformations syndrome.
AlAbdi L, Neuhann T, Prott EC, Schön U, Abdulwahab F, Faqeih E, Alkuraya FS. Hum Genet. 2024 Jun; 143(6):739-745. Epub 2024 May 14.
Characteristics and literature review of ETV6::ABL1 fusion gene-positive acute myeloid leukemia. [Int J Hematol. 2024]
Characteristics and literature review of ETV6::ABL1 fusion gene-positive acute myeloid leukemia.
Xue S, Sun HP, Huang XB, Chen X, Wang T, Ma W, Tian Y, Pan ZL, Li LH, Zhang L, et al. Int J Hematol. 2024 May; 119(5):564-572. Epub 2024 Mar 5.

RefSeq protein product
See the reference protein sequence for tyrosine-protein kinase ABL1 isoform b (NP_009297.2).

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Protein sequence from Nucleotide coding region
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Homo sapiens dematin actin binding protein (DMTN), transcript variant 2, mRNA
Homo sapiens dematin actin binding protein (DMTN), transcript variant 2, mRNA
gi|723802085|ref|NM_001114135.3|

Nucleotide

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Nucleotide