The protein encoded by this gene is a member of the FK506-binding protein family of peptidyl-prolyl cis-trans isomerases. The encoded protein is found in the lumen of the endoplasmic reticulum, where it is thought to accelerate protein folding. Defects in this gene are a cause of a type of Ehlers-Danlos syndrome (EDS). Both a protein-coding variant and noncoding variants are transcribed from this gene. [provided by RefSeq, Mar 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FKBP14-20-RE | 20 (40 μL) | 200 μL |  |
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| FKBP14-20-OR | 20 (40 μL) | 200 μL |  |
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| FKBP14-20-GO | 20 (40 μL) | 200 μL |  |
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| FKBP14-20-GR | 20 (40 μL) | 200 μL |  |
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| FKBP14-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a member of the FK506-binding protein family of peptidyl-prolyl cis-trans isomerases. The encoded protein is found in the lumen of the endoplasmic reticulum, where it is thought to accelerate protein folding. Defects in this gene are a cause of a type of Ehlers-Danlos syndrome (EDS). Both a protein-coding variant and noncoding variants are transcribed from this gene. [provided by RefSeq, Mar 2012]
Gene Symbol : FKBP14
Gene Name : FK506 binding protein 14
Chromosome : CHR 7: 300,268,00-300,105,82
Locus : 7p14.3
Alt. Genes : DNAL4
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