Target Name: SCARNA4
NCBI ID: G677771
Review Report on SCARNA4 Target / Biomarker Content of Review Report on SCARNA4 Target / Biomarker
SCARNA4
Other Name(s): small Cajal body-specific RNA 4 | Small Cajal body-specific RNA 4 | ACA26

SCARNA4: A Potential Drug Target and Biomarker for Small Cajal Body-Specific RNA 4

Small Cajal body-specific RNA 4 (SCARNA4) is a non-coding RNA molecule that has been identified in various organisms, including humans. It plays a crucial role in the development and maintenance of tissues, including brain and spinal cord. The identification of SCARNA4 as a potential drug target and biomarker has significant implications for the study of neurodegenerative diseases.

The Cajal body

The Cajal body is a type of RNA molecule that is found in various organisms, including humans. It is characterized by the presence of a specific stem-loop region and is involved in the regulation of gene expression. SCARNA4 is a member of the Cajal body family and is expressed in a variety of tissues, including brain, heart, and muscle.

Function and regulation

SCARNA4 is involved in the regulation of gene expression and has been shown to play a role in various cellular processes, including cell growth, differentiation, and inflammation. It is also involved in the development and maintenance of tissues, including the brain and spinal cord.

In addition to its role in cell regulation, SCARNA4 has also been shown to play a role in the development of neurodegenerative diseases. The neurodegenerative diseases, such as Alzheimer's disease, Parkinson's disease, and Huntington's disease, are characterized by the progressive loss of brain cells and the development of characteristic symptoms.

Drug targeting

The potential drug targeting of SCARNA4 is based on its involvement in the regulation of gene expression and its role in the development of neurodegenerative diseases. Drugs that target SCARNA4 have the potential to treat neurodegenerative diseases by modulating its expression and function.

One approach to drug targeting is to use small molecules that can interact with SCARNA4 and modulate its activity. This approach has been used to develop drugs for various neurological disorders, including Alzheimer's disease and Parkinson's disease.

Another approach to drug targeting is to use RNA interference (RNAi) technology to knockdown SCARNA4 expression in target cells. This approach has been used to study the role of SCARNA4 in various cellular processes and to identify potential drug targets.

Biomarker

SCARNA4 has also been identified as a potential biomarker for neurodegenerative diseases. The development of biomarkers for neurodegenerative diseases has significant implications for the diagnosis and treatment of these disorders.

The identification of SCARNA4 as a potential biomarker for neurodegenerative diseases has been shown by various studies, including gene expression profiling and the use of antibodies that recognize SCARNA4. These studies have identified SCARNA4 as a reliable and sensitive biomarker for the diagnosis and treatment of neurodegenerative diseases.

Conclusion

In conclusion, SCARNA4 is a non-coding RNA molecule that is involved in the regulation of gene expression and the development and maintenance of tissues, including the brain and spinal cord. Its potential as a drug target and biomarker for neurodegenerative diseases has significant implications for the study of these disorders and the development of new treatments. Further research is needed to fully understand the role of SCARNA4 in the development and treatment of neurodegenerative diseases.

Protein Name: Small Cajal Body-specific RNA 4

The "SCARNA4 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 SCARNA4 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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