Difference between revisions of "YJR035W"
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| − | '''Description of YJR035W:''' Protein involved in transcription-coupled nucleotide excision repair of UV-induced DNA lesions; recruitment to DNA lesions is dependent on an elongating RNA polymerase II; homolog of human CSB protein<ref name='S000070015'>Lee SK, et al. (2002) Yeast RAD26, a homolog of the human CSB gene, functions independently of nucleotide excision repair and base excision repair in promoting transcription through damaged bases. Mol Cell Biol 22(12):4383-9 {{SGDpaper|S000070015}} PMID 12024048</ref><ref name='S000132521'>Malik S, et al. ( | + | '''Description of YJR035W:''' Protein involved in transcription-coupled nucleotide excision repair of UV-induced DNA lesions; recruitment to DNA lesions is dependent on an elongating RNA polymerase II; homolog of human CSB protein<ref name='S000070015'>Lee SK, et al. (2002) Yeast RAD26, a homolog of the human CSB gene, functions independently of nucleotide excision repair and base excision repair in promoting transcription through damaged bases. Mol Cell Biol 22(12):4383-9 {{SGDpaper|S000070015}} PMID 12024048</ref><ref name='S000132521'>Malik S, et al. (2010) Rad26p, a transcription-coupled repair factor, is recruited to the site of DNA lesion in an elongating RNA polymerase II-dependent manner in vivo. Nucleic Acids Res 38(5):1461-77 |
{{SGDpaper|S000132521}} PMID 20007604</ref> | {{SGDpaper|S000132521}} PMID 20007604</ref> | ||
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Revision as of 13:05, 13 March 2010
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| Systematic name | YJR035W |
| Gene name | RAD26 |
| Aliases | |
| Feature type | ORF, Verified |
| Coordinates | Chr X:497347..500604 |
| Primary SGDID | S000003796 |
Description of YJR035W: Protein involved in transcription-coupled nucleotide excision repair of UV-induced DNA lesions; recruitment to DNA lesions is dependent on an elongating RNA polymerase II; homolog of human CSB protein[1][2]
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References
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- ↑ Lee SK, et al. (2002) Yeast RAD26, a homolog of the human CSB gene, functions independently of nucleotide excision repair and base excision repair in promoting transcription through damaged bases. Mol Cell Biol 22(12):4383-9 SGD PMID 12024048
- ↑ Malik S, et al. (2010) Rad26p, a transcription-coupled repair factor, is recruited to the site of DNA lesion in an elongating RNA polymerase II-dependent manner in vivo. Nucleic Acids Res 38(5):1461-77 SGD PMID 20007604
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