The protein encoded by this gene is a bifunctional enzyme that channels 1-carbon units from formiminoglutamate, a metabolite of the histidine degradation pathway, to the folate pool. Mutations in this gene are associated with glutamate formiminotransferase deficiency. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Dec 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FTCD-20-RE | 20 (40 μL) | 200 μL |  |
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| FTCD-20-OR | 20 (40 μL) | 200 μL |  |
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| FTCD-20-GO | 20 (40 μL) | 200 μL |  |
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| FTCD-20-GR | 20 (40 μL) | 200 μL |  |
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| FTCD-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a bifunctional enzyme that channels 1-carbon units from formiminoglutamate, a metabolite of the histidine degradation pathway, to the folate pool. Mutations in this gene are associated with glutamate formiminotransferase deficiency. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Dec 2009]
Gene Symbol : FTCD
Gene Name : Formimidoyltransferase cyclodeaminase
Chromosome : CHR 21: 461,564,80-461,359,80
Locus : 21q22.3
Alt. Genes : OPTN
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