The protein encoded by this gene plays a crucial role in B-cell development. Mutations in this gene cause X-linked agammaglobulinemia type 1, which is an immunodeficiency characterized by the failure to produce mature B lymphocytes, and associated with a failure of Ig heavy chain rearrangement. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2013]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| BTKBA-20-REGO | 20 (40 μL) | 200 μL |
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| BTKBA-20-REGR | 20 (40 μL) | 200 μL |
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| BTKBA-20-ORGR | 20 (40 μL) | 200 μL |
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| BTKBA-20-GOGR | 20 (40 μL) | 200 μL |
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| BTKBA-20-GRRE | 20 (40 μL) | 200 μL |
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| BTKBA-20-GROR | 20 (40 μL) | 200 μL |
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| BTKBA-20-GRGO | 20 (40 μL) | 200 μL |
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| BTKBA-20-AQOR | 20 (40 μL) | 200 μL |
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The protein encoded by this gene plays a crucial role in B-cell development. Mutations in this gene cause X-linked agammaglobulinemia type 1, which is an immunodeficiency characterized by the failure to produce mature B lymphocytes, and associated with a failure of Ig heavy chain rearrangement. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2013]
Gene Symbol : BTK
Gene Name : Bruton tyrosine kinase
Chromosome : CHR X: 101,390,795-101,349,446
Locus : Xq22.1
Alt. Genes : HIPK3
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