This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene can cause non-syndromic deafness or erythrokeratodermia variabilis, a skin disorder. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| GJB3BA-20-REGO | 20 (40 μL) | 200 μL |
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| GJB3BA-20-REGR | 20 (40 μL) | 200 μL |
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| GJB3BA-20-ORGR | 20 (40 μL) | 200 μL |
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| GJB3BA-20-GOGR | 20 (40 μL) | 200 μL |
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| GJB3BA-20-GRRE | 20 (40 μL) | 200 μL |
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| GJB3BA-20-GROR | 20 (40 μL) | 200 μL |
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| GJB3BA-20-GRGO | 20 (40 μL) | 200 μL |
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| GJB3BA-20-AQOR | 20 (40 μL) | 200 μL |
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This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene can cause non-syndromic deafness or erythrokeratodermia variabilis, a skin disorder. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]
Gene Symbol : GJB3
Gene Name : Gap junction protein beta 3
Chromosome : CHR 1: 347,811,88-347,863,65
Locus : 1p34.3
Alt. Genes : CEBPZ
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