Target Name: RAD17P2
NCBI ID: G9206
Review Report on RAD17P2 Target / Biomarker Content of Review Report on RAD17P2 Target / Biomarker
RAD17P2
Other Name(s): RAD17 pseudogene 2 | RAD17 homolog (S. pombe) pseudogene 2 | HRAD17P2

Exploring The Potential of RAD17P2 as A Drug Target

RAD17P2 (RAD17 pseudogene 2) is a gene that encodes a protein known as RAD17, which plays a critical role in the regulation of DNA double-strand break repair. The RAD17 gene is located on chromosome 17 and has been implicated in a variety of cellular processes, including DNA repair, cell cycle progression, and apoptosis.

Despite the significant research that has been conducted on the RAD17 gene, much of its function and potential as a drug target remains unexplored. In this article, we will explore the biology of RAD17P2 and its potential as a drug target, with a focus on its function in the context of human disease.

The RAD17 gene and its function

The RAD17 gene is a member of the T-DNA gene family, which encodes proteins involved in the transfer of DNA sequences between cells. The RAD17 gene is located on chromosome 17 and has been shown to encode a protein with multiple functions in the cell.

One of the most significant functions of RAD17 is its role in DNA double-strand break repair. DNA double-strand breaks are a common type of genetic mutation that can occur during DNA replication, transcription, or repair. These breaks can result in the loss or disruption of gene function, and can lead to the development of a variety of diseases, including cancer.

The RAD17 protein plays a critical role in the regulation of DNA double-strand break repair by ensuring that damaged DNA is accurately repaired and that repair pathways are properly activated. This is accomplished through the formation of a complex between the RAD17 protein and the DNA repair machinery.

In addition to its role in DNA repair, RAD17 has also been shown to play a critical role in cell cycle progression and apoptosis. The RAD17 protein is involved in the regulation of the G1/S transition, which is a critical step in the cell cycle and is associated with the growth and development of cancer.

The potential as a drug target

The potential drug targeting of RAD17P2 is due to its unique function in the regulation of DNA double-strand break repair and its involvement in the development of a variety of diseases.

One approach to targeting RAD17P2 as a drug is to use small molecules that can modulate its activity. For example, there is a growing body of research on the use of small molecules as drugs for the treatment of cancer, and RAD17P2 is an attractive target due to its involvement in this process.

Another approach to targeting RAD17P2 is to use antibodies that can specifically recognize and target the RAD17P2 protein. This approach has the advantage of being highly specific and can be used to measure the activity of RAD17P2 in a variety of cellular contexts.

Conclusion

In conclusion, RAD17P2 is a gene that has significant potential as a drug target due to its involvement in the regulation of DNA double-strand break repair and its association with the development of a variety of diseases. The use of small molecules and antibodies as drug vehicles has the potential to further our understanding of the biology of RAD17P2 and its role in the development of human disease. Further research is needed to fully explore the potential of RAD17P2 as a drug target and to develop effective treatments for the treatment of cancer and other diseases.

Protein Name: RAD17 Pseudogene 2

The "RAD17P2 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about RAD17P2 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

More Common Targets

RAD18 | RAD21 | RAD21-AS1 | RAD21L1 | RAD23A | RAD23B | RAD50 | RAD51 | RAD51-AS1 | RAD51AP1 | RAD51AP2 | RAD51B | RAD51C | RAD51D | RAD51L3-RFFL | RAD52 | RAD54B | RAD54L | RAD54L2 | RAD9A | RAD9B | RADIL | RADX | RAE1 | RAET1E | RAET1E-AS1 | RAET1G | RAET1K | RAET1L | Raf kinase | RAF1 | RAF1P1 | RAG1 | RAG2 | Ragulator Complex | RAI1 | RAI14 | RAI2 | RALA | RALB | RALBP1 | RALBP1P1 | RalGAP1 complex | RALGAPA1 | RALGAPA2 | RALGAPB | RALGDS | RALGPS1 | RALGPS2 | RALY | RALYL | RAMAC | RAMACL | RAMP1 | RAMP2 | RAMP2-AS1 | RAMP3 | RAN | RANBP1 | RANBP10 | RANBP17 | RANBP1P1 | RANBP2 | RANBP3 | RANBP3-DT | RANBP3L | RANBP6 | RANBP9 | RANGAP1 | RANGRF | RANP1 | RANP6 | RAP1A | RAP1B | RAP1BL | RAP1GAP | RAP1GAP2 | RAP1GDS1 | RAP2A | RAP2B | RAP2C | RAP2C-AS1 | RAPGEF1 | RAPGEF2 | RAPGEF3 | RAPGEF4 | RAPGEF4-AS1 | RAPGEF5 | RAPGEF6 | RAPGEFL1 | RAPH1 | RAPSN | RARA | RARA-AS1 | RARB | RARG | RARRES1 | RARRES2 | RARS1 | RARS2