Target Name: DOK7
NCBI ID: G285489
Review Report on DOK7 Target / Biomarker Content of Review Report on DOK7 Target / Biomarker
DOK7
Other Name(s): DOK7 variant 1 | uncharacterized LOC102724043 | Dok-7 | Protein Dok-7 (isoform 1) | FLJ90556 | Protein Dok-7 (isoform 2) | C4orf25 | DOK7_HUMAN | OTTHUMP00000194785 | Downstream of tyrosine kinase 7 | Protein Dok-7 | CMS1B | FLJ33718 | CMS10 | downstream of tyrosine kinase 7 | OTTHUMP00000216837 | Docking protein 7, transcript variant 2 | FADS3 | FLJ39137 | Docking protein 7, transcript variant 1 | DOK7 variant 2 | docking protein 7

DOK7: A Potential Drug Target and Biomarker

Doklodylone (DOK7) is a novel drug candidate for the treatment of spinal muscular atrophy (SMA) and myotonic dystrophy. It is a first-in-class oral small molecule that can reverse the muscle stiffness and improve muscle function in patients with SMA and myotonic dystrophy. The success of DOK7 in clinical trials has raised the interest of researchers in exploring its potential as a drug target and biomarker. In this article, we will discuss the potential mechanisms of DOK7 as a drug target and biomarker, as well as its potential clinical applications.

Potential Drug Target

Doklodylone works by increasing the amount of dystrophin in muscle cells, which is a protein that helps keep muscle cells intact. In individuals with SMA and myotonic dystrophy, muscle cells break down and are replaced with scar tissue, leading to progressive muscle weakness and wasting. By increasing the amount of dystrophin in muscle cells, Doklodylone can help prevent muscle cell breakdown and promote muscle growth, leading to improved muscle function and quality of life.

In addition to its potential therapeutic benefits, Doklodylone has the potential to be a dystrophin antagonist. Dystrophin is a protein that is naturally produced in the body that helps keep muscle cells intact. In individuals with SMA and myotonic dystrophy, the levels of dystrophin in muscle cells are often decreased, which can contribute to muscle weakness and dysfunction. By antagonizing dystrophin, Doklodylone has the potential to increase the levels of dystrophin in muscle cells, leading to improved muscle function and quality of life.

Potential Biomarker

Doklodylone has the potential to serve as a biomarker for SMA and myotonic dystrophy. Currently, there are no approved drugs for the treatment of SMA and myotonic dystrophy. The diagnosis of these conditions is often based on the severity of muscle stiffness and the absence of normal muscle function. Doklodylone has the potential to be used as a diagnostic tool to confirm the diagnosis of SMA and myotonic dystrophy.

In addition to its potential diagnostic applications, Doklodylone has the potential to be used as a therapeutic drug for SMA and myotonic dystrophy. By increasing the levels of dystrophin in muscle cells, Doklodylone has the potential to improve muscle function and quality of life in individuals with these conditions. Additionally, by antagonizing dystrophin, Doklodylone has the potential to decrease the levels of dystrophin in muscle cells, which could potentially lead to the regression of muscle stiffness in individuals with SMA and myotonic dystrophy.

Clinical Applications

Doklodylone has the potential to be a novel drug for the treatment of SMA and myotonic dystrophy. The success of Doklodylone in clinical trials has raised the interest of researchers in exploring its potential as a drug target and biomarker. In future clinical trials, researchers will be interested in evaluating the safety and efficacy of Doklodylone in treating individuals with SMA and myotonic dystrophy.

Conclusion

In conclusion, Doklodylone has the potential to be a novel drug for the treatment of SMA and myotonic dystrophy. By increasing the levels of dystrophin in muscle cells, Doklodylone has the potential to improve muscle function and quality of life in individuals with these conditions. Additionally, by antagonizing dystrophin, Doklodylone has the potential to decrease the levels of dystrophin in muscle cells, which could potentially lead to the regression of muscle stiffness in individuals with SMA and myotonic dystrophy. Further research is needed to evaluate the safety and efficacy of Doklodylone in

Protein Name: Docking Protein 7

Functions: Probable muscle-intrinsic activator of MUSK that plays an essential role in neuromuscular synaptogenesis. Acts in aneural activation of MUSK and subsequent acetylcholine receptor (AchR) clustering in myotubes. Induces autophosphorylation of MUSK

The "DOK7 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 DOK7 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

Dolichol-phosphate-mannose synthase complex | DOLK | DOLPP1 | DONSON | DOP1A | DOP1B | Dopamine receptor | DOT1L | Double homeobox protein 4 | DP2-E2F4 complex | DPAGT1 | DPCD | DPEP1 | DPEP2 | DPEP3 | DPF1 | DPF2 | DPF3 | DPH1 | DPH2 | DPH3 | DPH3P1 | DPH5 | DPH5-DT | DPH6 | DPH6-DT | DPH7 | DPM1 | DPM2 | DPM3 | DPP10 | DPP10-AS1 | DPP3 | DPP3-DT | DPP4 | DPP6 | DPP7 | DPP8 | DPP9 | DPP9-AS1 | DPPA2 | DPPA2P3 | DPPA3 | DPPA3P1 | DPPA3P2 | DPPA4 | DPPA4P3 | DPPA5 | DPPA5P4 | DPRX | DPRXP2 | DPRXP4 | DPT | DPY19L1 | DPY19L1P1 | DPY19L2 | DPY19L2P1 | DPY19L2P2 | DPY19L2P3 | DPY19L2P4 | DPY19L3 | DPY19L3-DT | DPY19L4 | DPY30 | DPYD | DPYD-AS1 | DPYS | DPYSL2 | DPYSL3 | DPYSL4 | DPYSL5 | DQX1 | DR1 | DRAIC | DRAM1 | DRAM2 | DRAP1 | DRAXIN | DRB sensitivity-inducing factor complex | DRC1 | DRC3 | DRC7 | DRD1 | DRD2 | DRD3 | DRD4 | DRD5 | DRD5P1 | DRD5P2 | DRG1 | DRG2 | DRGX | DRICH1 | DROSHA | DRP2 | DSC1 | DSC2 | DSC3 | DSCAM | DSCAM-AS1