Target Name: CLEC12A
NCBI ID: G160364
Review Report on CLEC12A Target / Biomarker Content of Review Report on CLEC12A Target / Biomarker
CLEC12A
Other Name(s): C-type lectin-like molecule 1 | CL12A_HUMAN | Dendritic cell-associated lectin 2 | dendritic cell-associated lectin 2 | Myeloid inhibitory C-type lectin-like receptor | C-type lectin domain family 12 member A, transcript variant 1 | CLL-1 | C-type lectin domain family 12 member A | CD371 | CLEC12A variant 1 | C-type lectin protein CLL-1 | myeloid inhibitory C-type lectin-like receptor | C-type lectin domain family 12 member A (isoform 1) | Dendritic cell associated lectin 2 | CLL1 | DCAL-2 | C-type lectin superfamily | C-type lectin-like molecule-1 | MICL

clec12a: a potential drug target and biomarker

CLEC12A is a C-type lectin-like molecule that has been identified as a potential drug target and biomarker. It is a protein that is expressed in various cell types, including epithelial, hematopoietic, and neural cells, and has been shown to play a role in cell signaling, adhesion, and migration. In this article, we will explore the potential implications of clec12a as a drug target and biomarker.

Potential Drug Target

CLEC12A has been shown to interact with several protein tyrosine kinases, including TAK-2, FAK, and Src. These interactions suggest that clec12a may be a useful target for small molecule inhibitors. In fact, several studies have shown that inhibitors of clec12a can inhibit the activity of these protein tyrosine kinases, leading to a reduction in cell proliferation and survival.

In addition, clec12a has also been shown to interact with and inhibit the activity of the protein FAK. This suggests that clec12a may be a potential inhibitor of FAK-mediated signaling pathways, which could be useful in the treatment of various diseases, including cancer.

Potential Biomarker

CLEC12A has also been shown to be expressed in various types of cancer, including breast, lung, and ovarian cancer. This suggests that clec12a may be a potential biomarker for cancer diagnosis and treatment. In addition, since clec12a is also expressed in normal cells, it may be a useful biomarker for monitoring the effectiveness of cancer treatments.

Anti-Inflammatory Activities

In addition to its potential drug and biomarker applications, clec12a has also been shown to have anti-inflammatory activities. Several studies have shown that clec12a can inhibit the production of pro-inflammatory cytokines, such as TNF-alpha, IL-1, and IL-6. This suggests that clec12a may be a potential therapeutic agent for the treatment of inflammatory diseases.

Clec12a has also been shown to interact with the protein IRAK4, which is involved in the production of pro-inflammatory cytokines. This suggests that clec12a may be a potential target for inhibitors of IRAK4, which could be useful in the treatment of inflammatory diseases.

Conclusion

In conclusion, clec12a is a C-type lectin-like molecule that has been shown to interact with several protein tyrosine kinases and has anti-inflammatory activities. These properties make clec12a a potential drug target and biomarker. Further research is needed to fully understand the role of clec12a in cell signaling and disease, and to determine its potential as a therapeutic agent.

Protein Name: C-type Lectin Domain Family 12 Member A

Functions: Cell surface receptor that modulates signaling cascades and mediates tyrosine phosphorylation of target MAP kinases

The "CLEC12A 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 CLEC12A 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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