Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the Y chromosome. [provided by RefSeq, Sep 2013]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ARSEBA-20-REGO | 20 (40 μL) | 200 μL |
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| ARSEBA-20-REGR | 20 (40 μL) | 200 μL |
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| ARSEBA-20-ORGR | 20 (40 μL) | 200 μL |
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| ARSEBA-20-GOGR | 20 (40 μL) | 200 μL |
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| ARSEBA-20-GRRE | 20 (40 μL) | 200 μL |
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| ARSEBA-20-GROR | 20 (40 μL) | 200 μL |
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| ARSEBA-20-GRGO | 20 (40 μL) | 200 μL |
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| ARSEBA-20-AQOR | 20 (40 μL) | 200 μL |
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Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the Y chromosome. [provided by RefSeq, Sep 2013]
Gene Symbol : ARSE
Gene Name : Arylsulfatase E (chondrodysplasia punctata 1)
Chromosome : CHR X: 296,830,9-293,463,1
Locus : Xp22.33
Alt. Genes : MPHOSPH9
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