FAM111B-GLYATL1 Fusion FISH Probe
The FAM111B-GLYATL1 Fusion FISH Probe is used to confirm a fusion of the FAM111B and GLYATL1 genes. The fusion of the FAM111B and GLYATL1 genes has been associated with Breast Invasive Carcinoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** This product is for in vitro and research use only. This product is not intended for diagnostic use. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
FAM111B-GLYATL1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-RERE | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-REOR | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-REGO | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-REGR | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-REAQ | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-ORRE | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-OROR | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-ORGO | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-ORAQ | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-GORE | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-GOOR | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-GOGO | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-GOGR | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-GOAQ | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-GRRE | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-GROR | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-GRGO | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-GRGR | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-GRAQ | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-AQRE | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-AQOR | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-AQGO | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-AQGR | 20 (40 μL) | 200 μL | ||
FAM111B-GLYATL1-20-AQAQ | 20 (40 μL) | 200 μL |
GLYATL1 Gene Summary
The Glycine-N-acyltransferase Like 1 (GLYATL1) gene is located on chr11 :58695101-58724543 at 11q12.1.
Gene Name: Glycine-N-acyltransferase Like 1
Chromosome: CHR11: 58695101 -58724543
Locus: 11q12.1
FAM111B Gene Summary
This gene encodes a protein with a trypsin-like cysteine/serine peptidase domain in the C-terminus. Mutations in this gene are associated with an autosomal dominant form of hereditary fibrosing poikiloderma (HFP). Affected individuals display mottled pigmentation, telangiectasia, epidermal atrophy, tendon contractures, and progressive pulmonary fibrosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms. A paralog of this gene which also has a trypsin‐like peptidase domain, FAM111A, is located only 16 kb from this gene on human chromosome 11q12.1. [provided by RefSeq, Apr 2014]
Gene Name: Family With Sequence Similarity 111 Member B
Chromosome: CHR11: 58874657 -58894888
Locus: 11q12.1
Gene Diseases
The FAM111B GLYATL1 Fusion has been associated with the following diseases:
Disease Name |
---|
Breast Invasive Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
---|