This gene encodes a putative transcriptional activator that is a member of the AF4\FMR2 gene family. This gene is associated with the folate-sensitive fragile X E locus on chromosome X. A repeat polymorphism in the fragile X E locus results in silencing of this gene causing Fragile X E syndrome. Fragile X E syndrome is a form of nonsyndromic X-linked cognitive disability. In addition, this gene contains 6-25 GCC repeats that are expanded to >200 repeats in the disease state. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Jul 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| AFF2BA-20-REGO | 20 (40 μL) | 200 μL |
|
Request Pricing |
| AFF2BA-20-REGR | 20 (40 μL) | 200 μL |
|
Request Pricing |
| AFF2BA-20-ORGR | 20 (40 μL) | 200 μL |
|
Request Pricing |
| AFF2BA-20-GOGR | 20 (40 μL) | 200 μL |
|
Request Pricing |
| AFF2BA-20-GRRE | 20 (40 μL) | 200 μL |
|
Request Pricing |
| AFF2BA-20-GROR | 20 (40 μL) | 200 μL |
|
Request Pricing |
| AFF2BA-20-GRGO | 20 (40 μL) | 200 μL |
|
Request Pricing |
| AFF2BA-20-AQOR | 20 (40 μL) | 200 μL |
|
Request Pricing |
This gene encodes a putative transcriptional activator that is a member of the AF4\FMR2 gene family. This gene is associated with the folate-sensitive fragile X E locus on chromosome X. A repeat polymorphism in the fragile X E locus results in silencing of this gene causing Fragile X E syndrome. Fragile X E syndrome is a form of nonsyndromic X-linked cognitive disability. In addition, this gene contains 6-25 GCC repeats that are expanded to >200 repeats in the disease state. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Jul 2016]
Gene Symbol : AFF2
Gene Name : AF4/FMR2 family member 2
Chromosome : CHR X: 148,500,618-149,000,662
Locus : Xq28
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.