ABL1 Chromosome 9

ABL proto-oncogene 1, non-receptor tyrosine kinase
53 variants 53 Health Risk

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What This Gene Does
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]
Gene Info
Gene Group
"SH2 domain containing|Abl family tyrosine kinases"
Locus Type
gene with protein product
Location
9q34.12
Ensembl
ENSG00000097007
Associated Conditions (14)
Inborn genetic diseases
Congenital heart defects and skeletal malformations syndrome
ABL1-related disorder
Moyamoya angiopathy
Leukemia
Philadelphia chromosome-positive
resistant to imatinib
Chronic myelogenous leukemia
BCR-ABL1 positive
Congenital heart disease
Abnormal skeletal morphology
Failure to thrive
Lip and oral cavity carcinoma
Microcephaly
Key Variants
All Variants (53)
RSID Category Clinical Significance Conditions
RS1186996487 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1258494852 Health Risk Conflicting classifications of pathogenicity
RS138167706 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS139597295 Health Risk Conflicting classifications of pathogenicity Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome
RS141101699 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS144448357 Health Risk Conflicting classifications of pathogenicity Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome
RS147510280 Health Risk Conflicting classifications of pathogenicity
RS150134901 Health Risk Conflicting classifications of pathogenicity
RS1830948350 Health Risk Conflicting classifications of pathogenicity Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome
RS201146085 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS201376463 Health Risk Conflicting classifications of pathogenicity
RS370989546 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS373527910 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS375730000 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS571264328 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS749413196 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS754252285 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS765181270 Health Risk Conflicting classifications of pathogenicity ABL1-related disorder, ABL1-related disorder
RS766145624 Health Risk Conflicting classifications of pathogenicity
RS766806729 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS767992609 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS768153649 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS769405342 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS770388931 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS770760322 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS778257562 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS907710981 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS971577563 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1355021408 Health Risk Likely pathogenic Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome
RS1830947762 Health Risk Likely pathogenic Moyamoya angiopathy, Moyamoya angiopathy
RS1830947813 Health Risk Likely pathogenic Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome
RS1831097846 Health Risk Likely pathogenic Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome
RS1831388695 Health Risk Likely pathogenic Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome
RS2132956266 Health Risk Likely pathogenic Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome
RS2133022634 Health Risk Likely pathogenic Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome
RS2490715483 Health Risk Likely pathogenic Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome
RS2490721921 Health Risk Likely pathogenic Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome
RS121913459 Health Risk Likely pathogenic; association Leukemia, Philadelphia chromosome-positive, resistant to imatinib
RS1060499548 Health Risk Pathogenic Congenital heart defects and skeletal malformations syndrome, Congenital heart disease, Abnormal skeletal morphology
RS121913449 Health Risk Pathogenic Lip and oral cavity carcinoma, Lip and oral cavity carcinoma
RS121913454 Health Risk Pathogenic Lip and oral cavity carcinoma, Lip and oral cavity carcinoma
RS121913456 Health Risk Pathogenic
RS121913457 Health Risk Pathogenic Chronic myelogenous leukemia, BCR-ABL1 positive, Chronic myelogenous leukemia
RS121913461 Health Risk Pathogenic Leukemia, Philadelphia chromosome-positive, resistant to imatinib
RS137853304 Health Risk Pathogenic Chronic myelogenous leukemia, BCR-ABL1 positive, Chronic myelogenous leukemia
RS2133017541 Health Risk Pathogenic Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome
RS387906516 Health Risk Pathogenic Leukemia, Philadelphia chromosome-positive, resistant to imatinib
RS387906517 Health Risk Pathogenic Leukemia, Philadelphia chromosome-positive, resistant to imatinib
RS1060499547 Health Risk Pathogenic/Likely pathogenic Failure to thrive, Congenital heart disease, Abnormal skeletal morphology
RS1831099962 Health Risk Pathogenic/Likely pathogenic ABL1-related disorder, ABL1-related disorder
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