This intronless gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. The protein encoded functions as a lens-specific transcription factor and plays an important role in vertebrate lens formation. Mutations in this gene are associated with anterior segment mesenchymal dysgenesis and congenital primary aphakia. [provided by RefSeq, Dec 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FOXE3BA-20-REGO | 20 (40 μL) | 200 μL |
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| FOXE3BA-20-REGR | 20 (40 μL) | 200 μL |
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| FOXE3BA-20-ORGR | 20 (40 μL) | 200 μL |
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| FOXE3BA-20-GOGR | 20 (40 μL) | 200 μL |
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| FOXE3BA-20-GRRE | 20 (40 μL) | 200 μL |
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| FOXE3BA-20-GROR | 20 (40 μL) | 200 μL |
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| FOXE3BA-20-GRGO | 20 (40 μL) | 200 μL |
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| FOXE3BA-20-AQOR | 20 (40 μL) | 200 μL |
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This intronless gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. The protein encoded functions as a lens-specific transcription factor and plays an important role in vertebrate lens formation. Mutations in this gene are associated with anterior segment mesenchymal dysgenesis and congenital primary aphakia. [provided by RefSeq, Dec 2009]
Gene Symbol : FOXE3
Gene Name : Forkhead box E3
Chromosome : CHR 1: 474,160,71-474,180,51
Locus : 1p33
Alt. Genes : BET1
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