The CLCN family of voltage-dependent chloride channel genes comprises nine members (CLCN1-7, Ka and Kb) which demonstrate quite diverse functional characteristics while sharing significant sequence homology. Chloride channel 4 has an evolutionary conserved CpG island and is conserved in both mouse and hamster. This gene is mapped in close proximity to APXL (Apical protein Xenopus laevis-like) and OA1 (Ocular albinism type I), which are both located on the human X chromosome at band p22.3. The physiological role of chloride channel 4 remains unknown but may contribute to the pathogenesis of neuronal disorders. Alternate splicing results in two transcript variants that encode different proteins. [provided by RefSeq, Mar 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CLCN4BA-20-REGO | 20 (40 μL) | 200 μL |
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| CLCN4BA-20-REGR | 20 (40 μL) | 200 μL |
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| CLCN4BA-20-ORGR | 20 (40 μL) | 200 μL |
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| CLCN4BA-20-GOGR | 20 (40 μL) | 200 μL |
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| CLCN4BA-20-GRRE | 20 (40 μL) | 200 μL |
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| CLCN4BA-20-GROR | 20 (40 μL) | 200 μL |
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| CLCN4BA-20-GRGO | 20 (40 μL) | 200 μL |
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| CLCN4BA-20-AQOR | 20 (40 μL) | 200 μL |
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The CLCN family of voltage-dependent chloride channel genes comprises nine members (CLCN1-7, Ka and Kb) which demonstrate quite diverse functional characteristics while sharing significant sequence homology. Chloride channel 4 has an evolutionary conserved CpG island and is conserved in both mouse and hamster. This gene is mapped in close proximity to APXL (Apical protein Xenopus laevis-like) and OA1 (Ocular albinism type I), which are both located on the human X chromosome at band p22.3. The physiological role of chloride channel 4 remains unknown but may contribute to the pathogenesis of neuronal disorders. Alternate splicing results in two transcript variants that encode different proteins. [provided by RefSeq, Mar 2012]
Gene Symbol : CLCN4
Gene Name : Chloride voltage-gated channel 4
Chromosome : CHR X: 101,569,44-102,376,59
Locus : Xp22.2
Alt. Genes : LRPPRC
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