The protein encoded by this gene is a possible transcriptional regulator involved in retinal development. Defects in this gene can be a cause of autosomal-recessive retinitis pigmentosa. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ZNF513-20-RE | 20 (40 μL) | 200 μL |  |
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| ZNF513-20-OR | 20 (40 μL) | 200 μL |  |
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| ZNF513-20-GO | 20 (40 μL) | 200 μL |  |
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| ZNF513-20-GR | 20 (40 μL) | 200 μL |  |
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| ZNF513-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a possible transcriptional regulator involved in retinal development. Defects in this gene can be a cause of autosomal-recessive retinitis pigmentosa. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]
Gene Symbol : ZNF513
Gene Name : Zinc finger protein 513
Chromosome : CHR 2: 273,808,65-273,772,30
Locus : 2p23.3
Alt. Genes : OPTN
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