| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TMEM216-KCNG3-20-RERE | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-REOR | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-REGO | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-REGR | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-REAQ | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-ORRE | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-OROR | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-ORGO | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-ORGR | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-ORAQ | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-GORE | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-GOOR | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-GOGO | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-GOGR | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-GOAQ | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-GRRE | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-GROR | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-GRGO | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-GRGR | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-GRAQ | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-AQRE | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-AQOR | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-AQGO | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-AQGR | 20 (40 μL) | 200 μL |
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| TMEM216-KCNG3-20-AQAQ | 20 (40 μL) | 200 μL |
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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 Symbol : TMEM216
Gene Name : Transmembrane protein 216
Chromosome : CHR 11: 613,916,86-613,988,62
Locus : 11q12.2
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 Symbol : KCNG3
Gene Name : Potassium voltage-gated channel modifier subfamily G member 3
Chromosome : CHR 2: 424,940,96-424,420,16
Locus : 2p21
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