NPHP4-FAM71B Fusion FISH Probe
The NPHP4-FAM71B Fusion FISH Probe is used to confirm a fusion of the NPHP4 and FAM71B genes. The fusion of the NPHP4 and FAM71B genes has been associated with Stomach Adenocarcinoma. 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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| NPHP4-FAM71B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-RERE | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-REOR | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-REGO | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-REGR | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-REAQ | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-ORRE | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-OROR | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-ORGO | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-ORAQ | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-GORE | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-GOOR | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-GOGO | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-GOGR | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-GOAQ | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-GRRE | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-GROR | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-GRGO | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-GRGR | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-GRAQ | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-AQRE | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-AQOR | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-AQGO | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-AQGR | 20 (40 μL) | 200 μL |
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| NPHP4-FAM71B-20-AQAQ | 20 (40 μL) | 200 μL |
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FAM71B Gene Summary
The Family With Sequence Similarity 71 Member B (FAM71B) gene is located on chr5 :156589343-156593279 at 5q33.3.
Gene Name: Family With Sequence Similarity 71 Member B
Chromosome: CHR5: 156589343 -156593279
Locus: 5q33.3
NPHP4 Gene Summary
This gene encodes a protein involved in renal tubular development and function. This protein interacts with nephrocystin, and belongs to a multifunctional complex that is localized to actin- and microtubule-based structures. Mutations in this gene are associated with nephronophthisis type 4, a renal disease, and with Senior-Loken syndrome type 4, a combination of nephronophthisis and retinitis pigmentosa. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]
Gene Name: Nephrocystin 4
Chromosome: CHR1: 5922869 -6052533
Locus: 1p36.31
Gene Diseases
The NPHP4 FAM71B Fusion has been associated with the following diseases:
| Disease Name |
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| Stomach Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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