This gene encodes a protein belonging to the RAF family of serine/threonine protein kinases. This protein plays a role in regulating the MAP kinase/ERK signaling pathway, which affects cell division, differentiation, and secretion. Mutations in this gene, most commonly the V600E mutation, are the most frequently identified cancer-causing mutations in melanoma, and have been identified in various other cancers as well, including non-Hodgkin lymphoma, colorectal cancer, thyroid carcinoma, non-small cell lung carcinoma, hairy cell leukemia and adenocarcinoma of lung. Mutations in this gene are also associated with cardiofaciocutaneous, Noonan, and Costello syndromes, which exhibit overlapping phenotypes. A pseudogene of this gene has been identified on the X chromosome. [provided by RefSeq, Aug 2017]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
BRAF-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
BRAF-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
BRAF-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
BRAF-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
BRAF-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes a protein belonging to the RAF family of serine/threonine protein kinases. This protein plays a role in regulating the MAP kinase/ERK signaling pathway, which affects cell division, differentiation, and secretion. Mutations in this gene, most commonly the V600E mutation, are the most frequently identified cancer-causing mutations in melanoma, and have been identified in various other cancers as well, including non-Hodgkin lymphoma, colorectal cancer, thyroid carcinoma, non-small cell lung carcinoma, hairy cell leukemia and adenocarcinoma of lung. Mutations in this gene are also associated with cardiofaciocutaneous, Noonan, and Costello syndromes, which exhibit overlapping phenotypes. A pseudogene of this gene has been identified on the X chromosome. [provided by RefSeq, Aug 2017]
Gene Symbol : BRAF
Gene Name : B-Raf proto-oncogene, serine/threonine kinase
Chromosome : CHR 7: 140,924,763-140,719,330
Locus : 7q34
Alt. Genes : ZNF263
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