FRA12A is a folate-sensitive chromosomal fragile site prone to breakage. Though FRA12A can be inherited without phenotypic effect, patients with over 40% of their cells expressing FRA12A exhibit intellectual disability with or without other anomalies. An association between intellectual disability and a methylated polymorphic CGG trinucleotide repeat in the 5' untranslated region of a gene in the FRA12A region has been demonstrated. [provided by RefSeq, Jul 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FRA12ABA-20-REGO | 20 (40 μL) | 200 μL |
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| FRA12ABA-20-REGR | 20 (40 μL) | 200 μL |
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| FRA12ABA-20-ORGR | 20 (40 μL) | 200 μL |
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| FRA12ABA-20-GOGR | 20 (40 μL) | 200 μL |
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| FRA12ABA-20-GRRE | 20 (40 μL) | 200 μL |
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| FRA12ABA-20-GROR | 20 (40 μL) | 200 μL |
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| FRA12ABA-20-GRGO | 20 (40 μL) | 200 μL |
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| FRA12ABA-20-AQOR | 20 (40 μL) | 200 μL |
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FRA12A is a folate-sensitive chromosomal fragile site prone to breakage. Though FRA12A can be inherited without phenotypic effect, patients with over 40% of their cells expressing FRA12A exhibit intellectual disability with or without other anomalies. An association between intellectual disability and a methylated polymorphic CGG trinucleotide repeat in the 5' untranslated region of a gene in the FRA12A region has been demonstrated. [provided by RefSeq, Jul 2017]
Gene Symbol : FRA12A
Gene Name : Fragile site, folic acid type, rare, fra(12)(q13.1)
Chromosome : CHR 12: 0-0
Locus : 12q13.1
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