Target Name: CT47A12
NCBI ID: G100507170
Review Report on CT47A12 Target / Biomarker Content of Review Report on CT47A12 Target / Biomarker
CT47A12
Other Name(s): Cancer/testis antigen 47 | cancer/testis antigen 47A family member | CT47A_HUMAN | cancer/testis CT47 family, member 12 | cancer/testis antigen 47 | CT47 | CT47.12 | Cancer/testis antigen 47A | cancer/testis antigen family 47 member A12 | Cancer/testis CT47 family, member 8 | Cancer/testis antigen family 47, member A12

CT47A12: A Drug Target / Disease Biomarker

CT47A12 is a protein that is expressed in various tissues throughout the body, including the brain, spleen, and thymus. It is a member of the transforming growth factor beta (TGF-β) family, which is known for its role in cell growth, differentiation, and survival.

One of the most interesting aspects of CT47A12 is its potential as a drug target. The TGF-β family has been implicated in the development and progression of many diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. As such, CT47A12 has been identified as a potential target for a variety of therapeutic approaches, including small molecule inhibitors, monoclonal antibodies, and protein-based therapeutics.

One approach to targeting CT47A12 is to use small molecule inhibitors. These drugs work by binding to specific residues on the protein, inhibiting its activity and potentially leading to its degradation. There are currently several small molecule inhibitors that are being developed as potential treatments for diseases associated with TGF-β signaling, including cancer, neurodegenerative diseases, and autoimmune disorders.

Another approach to targeting CT47A12 is to use monoclonal antibodies. These drugs are designed to bind to a specific protein and can be used to either activate or inhibit its activity. Monoclonal antibodies have the potential to be highly specific and effective, as they can be designed to recognize and target specific residues on the protein. There are currently several monoclonal antibodies that are being developed as potential treatments for diseases associated with TGF-β signaling, including cancer, neurodegenerative diseases, and autoimmune disorders.

Another approach to targeting CT47A12 is to use protein-based therapeutics. These drugs are designed to be derived from proteins that have been expressed and purified from a variety of sources, including the brain, spleen, and thymus. This allows them to have a more natural and body-like composition, which can be beneficial in terms of safety and efficacy. There are currently several protein-based therapeutics that are being developed as potential treatments for diseases associated with TGF-β signaling, including cancer, neurodegenerative diseases, and autoimmune disorders.

In conclusion, CT47A12 is a protein that has significant potential as a drug target. Its association with the TGF-β family and its role in the development and progression of various diseases make it an attractive target for small molecule inhibitors, monoclonal antibodies, and protein-based therapeutics. As such, there is ongoing research into the development of compounds that can specifically target CT47A12 and potentially lead to new treatments for a variety of diseases.

Protein Name: Cancer/testis Antigen Family 47 Member A12

The "CT47A12 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 CT47A12 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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