The protein encoded by this gene functions together with DNA ligase IV and the DNA-dependent protein kinase in the repair of DNA double-strand breaks. This protein plays a role in both non-homologous end joining and the completion of V(D)J recombination. Mutations in this gene can cause short stature, microcephaly, and endocrine dysfunction (SSMED). Alternative splicing generates several transcript variants. [provided by RefSeq, Dec 2015]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| XRCC4-20-RE | 20 (40 μL) | 200 μL |  |
Request Pricing |
| XRCC4-20-OR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| XRCC4-20-GO | 20 (40 μL) | 200 μL |  |
Request Pricing |
| XRCC4-20-GR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| XRCC4-20-AQ | 20 (40 μL) | 200 μL |  |
Request Pricing |
The protein encoded by this gene functions together with DNA ligase IV and the DNA-dependent protein kinase in the repair of DNA double-strand breaks. This protein plays a role in both non-homologous end joining and the completion of V(D)J recombination. Mutations in this gene can cause short stature, microcephaly, and endocrine dysfunction (SSMED). Alternative splicing generates several transcript variants. [provided by RefSeq, Dec 2015]
Gene Symbol : XRCC4
Gene Name : X-ray repair cross complementing 4
Chromosome : CHR 5: 830,774,08-833,703,32
Locus : 5q14.2
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.