Difference between revisions of "ABL1"
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==Gene Overview== | ==Gene Overview== | ||
− | The ABL1 gene encodes for a non-receptor tyrosine kinase that is ubiquitously expressed and involved in a large number of cellular processes (see '''[https://www.ncbi.nlm.nih.gov/gene/25#reference-sequences "NCBI Gene]'''). A reciprocal translocation between chromosome 22 (BCR locus) and chromosome 9 (ABL1 locus) produces the Philadelphia chromosome, which is prevalent in chronic myeloid leukemia ( | + | The ABL1 gene encodes for a non-receptor tyrosine kinase that is ubiquitously expressed and involved in a large number of cellular processes (see '''[https://www.ncbi.nlm.nih.gov/gene/25#reference-sequences "NCBI Gene]'''). A reciprocal translocation between chromosome 22 (BCR locus) and chromosome 9 (ABL1 locus) produces the Philadelphia chromosome, which is prevalent in chronic myeloid leukemia (1, 2). |
==Common Alteration Types== | ==Common Alteration Types== |
Revision as of 11:43, 21 June 2018
Primary Author(s)*
Brian Davis, PhD
Synonyms
ABL proto-oncogene 1 non-receptor tyrosine kinase, Abelson tyrosine-protein kinase 1, ABL, JTK7, p150, c-ABL, v-abl, CHDSKM, c-ABL1; bcr/abl
Genomic Location
Cytoband: 9q34.12
Genomic Coordinates:
chr9:130,713,881-130,887,675(GRCh38/hg38)
chr9:133,589,268-133,763,062(GRCh37/hg19)
Cancer Category/Type
Chronic Myeloid Leukemia (also referred as (Chronic Myelogenous Leukemia)
Approximately 100% of patients diagnosed with Chronic Myeloid Leukemia ear a Philadelphia chromosome, which is a reciprocal translocation between chromosome 22 (BCR locus) and chromosome 9 (ABL1 locus).
Acute Lymphoid Leukemia
Gene Overview
The ABL1 gene encodes for a non-receptor tyrosine kinase that is ubiquitously expressed and involved in a large number of cellular processes (see "NCBI Gene). A reciprocal translocation between chromosome 22 (BCR locus) and chromosome 9 (ABL1 locus) produces the Philadelphia chromosome, which is prevalent in chronic myeloid leukemia (1, 2).
Common Alteration Types
Put your text here and/or fill in the table with an X where applicable
Copy Number Loss | Copy Number Gain | LOH | Loss-of-Function Mutation | Gain-of-Function Mutation | Translocation/Fusion |
---|---|---|---|---|---|
EXAMPLE: X | EXAMPLE: X | EXAMPLE: X | EXAMPLE: X | EXAMPLE: X | EXAMPLE: X |
Internal Pages
Put your text here
EXAMPLE Germline Cancer Predisposition Genes
External Links
Put your text here - Include as applicable links to: 1) Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2) COSMIC, 3) CIViC, 4) St. Jude ProteinPaint, 5) Precision Medicine Knnowledgebase (Weill Cornell), 6) Cancer Index, 7) OncoKB, 8) My Cancer Genome, 9) UniProt, 10) Pfam, 11) GeneCards, 12) GeneReviews, and 13) Any gene-specific databases.
EXAMPLES
ABL1 by Atlas of Genetics and Cytogenetics in Oncology and Haematology - detailed gene information
ABL1 by COSMIC - sequence information, expression, catalogue of mutations
ABL1 by CIViC - general knowledge and evidence-based variant specific information
ABL1 by St. Jude ProteinPaint mutational landscape and matched expression data.
ABL1 by Precision Medicine Knowledgebase (Weill Cornell) - manually vetted interpretations of variants and CNVs
ABL1 by Cancer Index - gene, pathway, publication information matched to cancer type
ABL1 by OncoKB - mutational landscape, mutation effect, variant classification
ABL1 by My Cancer Genome - brief gene overview
ABL1 by UniProt - protein and molecular structure and function
ABL1 by Pfam - gene and protein structure and function information
ABL1 by GeneCards - general gene information and summaries
"ABL1" by NCBI Gene - general gene information
References
1. Drucker, BJ et al. (2001). Activity of a Specific Inhibitor of the BCR-ABL Tyrosine Kinase in the Blast Crisis of Chronic Myeloid Leukemia and Acute Lymphoblastic Leukemia with the Philadelphia Chromosome. NEJM 344:1038-1042 PMID 11287973. DOI: 10.1056/NEJM200104053441402
2. Faderl, S et al. (1999). The Biology of Chronic Myeloid Leukemia. NEJM 341:164-172. PMID 10403855. DOI: 10.1056/NEJM199907153410306
3.
Notes
*Primary authors will typically be those that initially create and complete the content of a page. If a subsequent user modifies the content and feels the effort put forth is of high enough significance to warrant listing in the authorship section, please contact the CCGA coordinators (contact information provided on the homepage). Additional global feedback or concerns are also welcome.