This gene encodes a member of the fascin protein family. Fascins crosslink actin into filamentous bundles within dynamic cell extensions. This family member is proposed to play a role in photoreceptor disk morphogenesis. A mutation in this gene results in one form of autosomal dominant retinitis pigmentosa and macular degeneration. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FSCN2-20-RE | 20 (40 μL) | 200 μL |  |
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| FSCN2-20-OR | 20 (40 μL) | 200 μL |  |
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| FSCN2-20-GO | 20 (40 μL) | 200 μL |  |
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| FSCN2-20-GR | 20 (40 μL) | 200 μL |  |
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| FSCN2-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the fascin protein family. Fascins crosslink actin into filamentous bundles within dynamic cell extensions. This family member is proposed to play a role in photoreceptor disk morphogenesis. A mutation in this gene results in one form of autosomal dominant retinitis pigmentosa and macular degeneration. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Symbol : FSCN2
Gene Name : Fascin actin-bundling protein 2, retinal
Chromosome : CHR 17: 815,130,18-815,371,29
Locus : 17q25.3
Alt. Genes : CLEC3A
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