This gene encodes a single-strand specific DNA endonuclease that makes the 3' incision in DNA excision repair following UV-induced damage. The protein may also function in other cellular processes, including RNA polymerase II transcription, and transcription-coupled DNA repair. Mutations in this gene cause xeroderma pigmentosum complementation group G (XP-G), which is also referred to as xeroderma pigmentosum VII (XP7), a skin disorder characterized by hypersensitivity to UV light and increased susceptibility for skin cancer development following UV exposure. Some patients also develop Cockayne syndrome, which is characterized by severe growth defects, cognitive disability, and cachexia. Read-through transcription exists between this gene and the neighboring upstream BIVM (basic, immunoglobulin-like variable motif containing) gene. [provided by RefSeq, Feb 2011]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ERCC5BA-20-REGO | 20 (40 μL) | 200 μL |
|
Request Pricing |
| ERCC5BA-20-REGR | 20 (40 μL) | 200 μL |
|
Request Pricing |
| ERCC5BA-20-ORGR | 20 (40 μL) | 200 μL |
|
Request Pricing |
| ERCC5BA-20-GOGR | 20 (40 μL) | 200 μL |
|
Request Pricing |
| ERCC5BA-20-GRRE | 20 (40 μL) | 200 μL |
|
Request Pricing |
| ERCC5BA-20-GROR | 20 (40 μL) | 200 μL |
|
Request Pricing |
| ERCC5BA-20-GRGO | 20 (40 μL) | 200 μL |
|
Request Pricing |
| ERCC5BA-20-AQOR | 20 (40 μL) | 200 μL |
|
Request Pricing |
This gene encodes a single-strand specific DNA endonuclease that makes the 3' incision in DNA excision repair following UV-induced damage. The protein may also function in other cellular processes, including RNA polymerase II transcription, and transcription-coupled DNA repair. Mutations in this gene cause xeroderma pigmentosum complementation group G (XP-G), which is also referred to as xeroderma pigmentosum VII (XP7), a skin disorder characterized by hypersensitivity to UV light and increased susceptibility for skin cancer development following UV exposure. Some patients also develop Cockayne syndrome, which is characterized by severe growth defects, cognitive disability, and cachexia. Read-through transcription exists between this gene and the neighboring upstream BIVM (basic, immunoglobulin-like variable motif containing) gene. [provided by RefSeq, Feb 2011]
Gene Symbol : ERCC5
Gene Name : ERCC excision repair 5, endonuclease
Chromosome : CHR 13: 102,845,840-102,876,000
Locus : 13q33.1
Alt. Genes : ZNF256
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.