ANKHD1-EIF4EBP3-GTF2I Fusion FISH Probe
The ANKHD1-EIF4EBP3-GTF2I Fusion FISH Probe is used to confirm a fusion of the ANKHD1-EIF4EBP3 and GTF2I genes. The fusion of the ANKHD1-EIF4EBP3 and GTF2I genes has been associated with Kidney Renal Clear Cell 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| ANKHD1-EIF4EBP3-GTF2I-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-RERE | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-REOR | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-REGO | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-REGR | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-REAQ | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-ORRE | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-OROR | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-ORGO | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-ORAQ | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-GORE | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-GOOR | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-GOGO | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-GOGR | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-GOAQ | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-GRRE | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-GROR | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-GRGO | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-GRGR | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-GRAQ | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-AQRE | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-AQOR | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-AQGO | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-AQGR | 20 (40 μL) | 200 μL |
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| ANKHD1-EIF4EBP3-GTF2I-20-AQAQ | 20 (40 μL) | 200 μL |
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GTF2I Gene Summary
This gene encodes a phosphoprotein containing six characteristic repeat motifs. The encoded protein binds to the initiator element (Inr) and E-box element in promoters and functions as a regulator of transcription. This locus, along with several other neighboring genes, is deleted in Williams-Beuren syndrome. There are many closely related genes and pseudogenes for this gene on chromosome 7. This gene also has pseudogenes on chromosomes 9, 13, and 21. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Jul 2013]
Gene Name: General Transcription Factor IIi
Chromosome: CHR7: 74072029 -74175022
Locus: 7q11.23
ANKHD1-EIF4EBP3 Gene Summary
The ANKHD1-EIF4EBP3 mRNA is an infrequent but naturally occurring readthrough transcript of the neighboring ANKHD1 and EIF4EBP3 genes. This readthrough transcript encodes a protein composed mostly of the multiple ankyrin repeats, single KH-domain protein, with its C-terminus encoded in a different reading frame from the shared portion of the EIF4EBP3 gene. The significance of this readthrough mRNA and the function of its protein product have not yet been determined. [provided by RefSeq, Nov 2009]
Gene Name: ANKHD1-EIF4EBP3 Readthrough
Chromosome: CHR5: 139781398 -139929163
Locus: 5q31.3
Gene Diseases
The ANKHD1-EIF4EBP3 GTF2I Fusion has been associated with the following diseases:
| Disease Name |
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| Kidney Renal Clear Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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