This gene is located in the candidate region for congenital heart disease (CHD) in Down syndrome (DS). It encodes a basic protein that functions as a receptor that promotes insertion of tail-anchored proteins in the endoplasmic reticulum membrane. This gene is located at a maternally-methylated differentially methylated region (DMR); however, its transcription may be biallelic, not imprinted. Alternative splicing results in different transcript variants. A pseudogene has been defined on chromosome 4. [provided by RefSeq, Apr 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| WRB-20-RE | 20 (40 μL) | 200 μL |  |
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| WRB-20-OR | 20 (40 μL) | 200 μL |  |
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| WRB-20-GO | 20 (40 μL) | 200 μL |  |
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| WRB-20-GR | 20 (40 μL) | 200 μL |  |
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| WRB-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is located in the candidate region for congenital heart disease (CHD) in Down syndrome (DS). It encodes a basic protein that functions as a receptor that promotes insertion of tail-anchored proteins in the endoplasmic reticulum membrane. This gene is located at a maternally-methylated differentially methylated region (DMR); however, its transcription may be biallelic, not imprinted. Alternative splicing results in different transcript variants. A pseudogene has been defined on chromosome 4. [provided by RefSeq, Apr 2017]
Gene Symbol : WRB
Gene Name : Tryptophan rich basic protein
Chromosome : CHR 21: 393,802,86-393,978,88
Locus : 21q22.2
Alt. Genes : FAM13A
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