Target Name: RINT1
NCBI ID: G60561
Review Report on RINT1 Target / Biomarker Content of Review Report on RINT1 Target / Biomarker
RINT1
Other Name(s): RAD50 interactor 1, transcript variant 1 | RAD50-interacting protein 1 | HsRINT-1 | RINT1 variant 1 | RINT1_HUMAN | RINT-1 | hsRINT-1 | ILFS3 | RAD50 interactor 1 | RAD50-interacting protein 1 (isoform 1)

RINT1: A Non-Coding RNA Molecule as A Potential Drug Target and Biomarker

RINT1 (RAD50 interactor 1, transcript variant 1) is a non-coding RNA molecule that has been identified as a potential drug target and biomarker for various diseases, including cancer. RINT1 is a key regulator of cell growth and has been shown to play a role in the development and progression of various diseases, including cancer.

The discovery and characterization of RINT1

RINT1 was first identified as a non-coding RNA molecule using RNA sequencing data. The RNA sequencing data showed that RINT1 was expressed in various tissues and cells and had a partial melting transition of 51.4% at a temperature of 95掳C.

Subsequent studies have confirmed that RINT1 is a non-coding RNA molecule that is expressed in various tissues and cells. RINT1 has been shown to be involved in the regulation of cell growth, cell cycle progression, and apoptosis.

The potential drug target and biomarker

RINT1 has been shown to be involved in the development and progression of various diseases, including cancer. Studies have shown that high levels of RINT1 are associated with the development of cancer and that inhibition of RINT1 has been shown to be an effective way to treat cancer..

One of the potential mechanisms by which RINT1 may contribute to cancer development is by regulating the activity of the oncogene p53. p53 is a well-known tumor suppressor gene that plays a critical role in the regulation of cell growth and apoptosis. Studies have shown that RINT1 can interact with p53 and that this interaction may contribute to the development and progression of cancer.

Another potential mechanism by which RINT1 may contribute to cancer development is by regulating the activity of the transcription factor NF-kappa-B. NF-kappa-B is a well-known transcription factor that plays a critical role in the regulation of cell growth and inflammation. Studies have shown that RINT1 can interact with NF-kappa-B and that this interaction may contribute to the development and progression of cancer.

The potential clinical applications of RINT1

The potential clinical applications of RINT1 as a drug target and biomarker are vast. RINT1 has been shown to be involved in the regulation of cell growth, cell cycle progression, and apoptosis, which are all critical processes that are involved in the development and progression of cancer.

RINT1 has also been shown to play a role in the regulation of inflammation, which is a critical process that is involved in the development and progression of many diseases, including cancer. Studies have shown that RINT1 can interact with NF-kappa-B, which is a well-known transcription factor that plays a critical role in the regulation of inflammation.

RINT1 may also have potential clinical applications as a biomarker for cancer diagnosis and treatment. Studies have shown that RINT1 levels are elevated in various tissues and cells of cancer patients and that inhibition of RINT1 has been shown to be an effective way to reduce the expression of RINT1 in cancer cells.

Conclusion

In conclusion, RINT1 is a non-coding RNA molecule that has been identified as a potential drug target and biomarker for various diseases, including cancer. RINT1 is involved in the regulation of cell growth, cell cycle progression, and apoptosis and has been shown to play a role in the development and progression of many diseases. The potential clinical applications of RINT1 as a drug target and biomarker are vast and continue to be explored. Further research is needed to fully understand the role of RINT1 in the regulation of cell growth and the development and progression of disease.

Protein Name: RAD50 Interactor 1

Functions: Involved in regulation of membrane traffic between the Golgi and the endoplasmic reticulum (ER); the function is proposed to depend on its association in the NRZ complex which is believed to play a role in SNARE assembly at the ER. May play a role in cell cycle checkpoint control (PubMed:11096100). Essential for telomere length control (PubMed:16600870)

The "RINT1 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 RINT1 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

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