" /> BCR/ABL1 Fusion Protein with ABL1 NP_005148.2:p.V299L - CISMeF





Preferred Label : BCR/ABL1 Fusion Protein with ABL1 NP_005148.2:p.V299L;

NCIt synonyms : BCR/ABL V299L Mutation; BCR-ABL Val299Leu Mutation; BCR/ABL Val299Leu Mutation; BCR/ABL1 V299L Mutation; BCR-ABL1 V299L Mutation; BCR/ABL1 Fusion Protein with NP_005148.2:p.Val299Leu; BCR/ABL1 Fusion Protein with ABL1 NP_005148.2:p.Val299Leu; BCR/ABL Fusion Protein with Val299Leu; BCR/ABL1 Val299Leu Mutation; BCR/ABL1 Fusion Protein with NP_005148.2:p.V299L; BCR-ABL1 Val299Leu Mutation; BCR/ABL Fusion Protein with V299L; BCR-ABL V299L Mutation; BCR::ABL1 Fusion Protein with ABL1 NP_005148.2:p.V299L;

NCIt related terms : V299L;

NCIt definition : A fusion protein encoded by the BCR/ABL1 fusion gene with ABL1 NM_005157.4:c.895G C or c.895G T mutation. This protein is comprised of the N-terminus of the breakpoint cluster region protein fused to almost the entire tyrosine-protein kinase ABL1 protein where the valine at position 299 of the ABL1 protein has been replaced by leucine.;

NCIt note : The position of the amino acid substitution is denoted by its location in the tyrosine-protein kinase ABL1 protein sequence (NCBI Reference Sequence: NP_005148.2) and not its location in the fusion protein.;

NCI Metathesaurus CUI : CL513792;

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02/05/2024


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