ABL1 Chromosome 9
ABL proto-oncogene 1, non-receptor tyrosine kinase
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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
RS1186996487
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1258494852
Conflicting classifications of pathogenicity
Health Risk
RS138167706
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS139597295
Conflicting classifications of pathogenicity
Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome
Health Risk
RS141101699
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS144448357
Conflicting classifications of pathogenicity
Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome
Health Risk
RS147510280
Conflicting classifications of pathogenicity
Health Risk
RS150134901
Conflicting classifications of pathogenicity
Health Risk
RS1830948350
Conflicting classifications of pathogenicity
Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome
Health Risk
RS201146085
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS201376463
Conflicting classifications of pathogenicity
Health Risk
RS370989546
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
All Variants (53)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS1831432715 | Health Risk | Pathogenic/Likely pathogenic | Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome |
| RS1831432776 | Health Risk | Pathogenic/Likely pathogenic | Congenital heart defects and skeletal malformations syndrome, Microcephaly, Congenital heart defects and skeletal malformations syndrome |
| RS1831433011 | Health Risk | Pathogenic/Likely pathogenic | Congenital heart defects and skeletal malformations syndrome, Congenital heart defects and skeletal malformations syndrome |