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ABL1 (NM_005157) - ABL proto-oncogene 1, non-receptor tyrosine kinase

Tyrosine-Protein Kinase Abl1 Isoform A

Mutations Visualisation

Protein summary

This is preferred isoform of ABL1 protein. View all 2 isoforms
ABL1: tyrosine-protein kinase ABL1 isoform a
Description:

This gene is a protooncogene that encodes a protein tyrosine kinase involved in a variety of cellular processes, including cell division, adhesion, differentiation, and response to stress. The activity of the protein is negatively regulated by its SH3 domain, whereby deletion of the region encoding this domain results in an oncogene. The ubiquitously expressed protein has DNA-binding activity that is regulated by CDC2-mediated phosphorylation, suggesting a cell cycle function. This gene has been found fused to a variety of translocation partner genes in various leukemias, most notably the t(9;22) translocation that results in a fusion with the 5' end of the breakpoint cluster region gene (BCR; MIM:151410). Alternative splicing of this gene results in two transcript variants, which contain alternative first exons that are spliced to the remaining common exons. [provided by RefSeq, Aug 2014].

Strand
+
Chromosome
9
Protein
1130 residues
All mutations
185
PTM sites
72
CDS
133,710,833 - 133,761,070
Transcription
133,710,641 - 133,763,062
54.69% of sequence is predicted to be disordered

External references

Mappings retrieved from NCBI & UniProt.
RefSeq
Entrez
gene: 25
UniProt
Ensembl