TMEM216-KCNG3 Fusion FISH Probe
The TMEM216-KCNG3 Fusion FISH Probe is used to confirm a fusion of the TMEM216 and KCNG3 genes. The fusion of the TMEM216 and KCNG3 genes has been associated with Colon 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 |
|---|---|---|---|---|
| TMEM216-KCNG3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-RERE | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-REOR | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-REGO | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-REGR | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-OROR | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-GORE | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-GROR | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| TMEM216-KCNG3-20-AQAQ | 20 (40 μL) | 200 μL |
|
TMEM216 Gene Summary
This locus encodes a transmembrane domain-containing protein. Mutations at this locus have been associated with Meckel-Gruber Syndrome Type 2, and Joubert Syndrome 2, also known as Cerebello-oculorenal Syndrome 2. [provided by RefSeq, Aug 2010]
Gene Name: Transmembrane Protein 216
Chromosome: CHR11: 61159831 -61166335
Locus: 11q12.2
KCNG3 Gene Summary
Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily G. This member is a gamma subunit functioning as a modulatory molecule. Alternative splicing results in two transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]
Gene Name: Potassium Voltage-gated Channel Modifier Subfamily G Member 3
Chromosome: CHR2: 42669156 -42721237
Locus: 2p21
Gene Diseases
The TMEM216 KCNG3 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Colon Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|