This gene maps to a location 100 kb centromeric of the repeat units on chromosome 4q35 which are deleted in facioscapulohumeral muscular dystrophy (FSHD). It is evolutionarily conserved and has related sequences on multiple human chromosomes but DNA sequence analysis did not reveal any homology to known genes. In vivo studies demonstrate the encoded protein is localized to the nucleolus. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FRG1BA-20-REGO | 20 (40 μL) | 200 μL |
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| FRG1BA-20-REGR | 20 (40 μL) | 200 μL |
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| FRG1BA-20-ORGR | 20 (40 μL) | 200 μL |
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| FRG1BA-20-GOGR | 20 (40 μL) | 200 μL |
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| FRG1BA-20-GRRE | 20 (40 μL) | 200 μL |
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| FRG1BA-20-GROR | 20 (40 μL) | 200 μL |
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| FRG1BA-20-GRGO | 20 (40 μL) | 200 μL |
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| FRG1BA-20-AQOR | 20 (40 μL) | 200 μL |
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This gene maps to a location 100 kb centromeric of the repeat units on chromosome 4q35 which are deleted in facioscapulohumeral muscular dystrophy (FSHD). It is evolutionarily conserved and has related sequences on multiple human chromosomes but DNA sequence analysis did not reveal any homology to known genes. In vivo studies demonstrate the encoded protein is localized to the nucleolus. [provided by RefSeq, Jul 2008]
Gene Symbol : FRG1
Gene Name : FSHD region gene 1
Chromosome : CHR 4: 189,940,818-189,963,203
Locus : 4q35.2
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