Target Name: DSCR4
NCBI ID: G10281
Review Report on DSCR4 Target / Biomarker Content of Review Report on DSCR4 Target / Biomarker
DSCR4
Other Name(s): Down syndrome critical region gene 4 | DSCR4_HUMAN | DCRB | Down syndrome critical region protein 4 | DSCRB | Down syndrome critical region 4 | Down syndrome critical region protein B

DSCR4: A Potential Drug Target and Biomarker for Down syndrome

Introduction

Down syndrome is a complex neurodevelopmental disorder that affects approximately 250,000 individuals worldwide, primarily affecting children. It is characterized by a range of developmental, cognitive, and physical impairments, including severe cognitive impairment, motor delays, and persistent behavioral problems. Despite the availability of Numerous therapeutic options for managing Down syndrome, the underlying etiology of the disorder remains largely unaddressed.

The critical region gene (CRG) 4 is a gene that has been identified as a potential drug target and biomarker for Down syndrome. It is located on chromosome 21, near the critical region, and is involved in the development and maintenance of various cellular processes. . The discovery of CRG4 as a potential drug target and biomarker for Down syndrome has significant implications for the treatment of this disorder.

Understanding the Role of CRG4 in Down syndrome

The study of Down syndrome has traditionally focused on its neurobiological and molecular underpinnings. Recent research has identified several gene expressions that are differentially expressed in Down syndrome compared to the general population. One of these genes is CRG4.

CRG4 is a gene that encodes a protein known as CRG4, which is involved in the development and maintenance of various cellular processes. It is expressed in a wide range of tissues and cells, including brain, heart, and skeletal muscles. Several studies have demonstrated that CRG4 is involved in the development and progression of Down syndrome.

One of the most significant findings is that CRG4 is expressed in the brains of individuals with Down syndrome, and is highly expressed in the prefrontal cortical regions of these individuals. This suggests that CRG4 may be involved in the pathophysiology of Down syndrome.

Another study found that CRG4 was expressed in the placenta of individuals with Down syndrome, which is the site of fetal development. This suggests that CRG4 may be involved in the development of Down syndrome.

Potential Therapeutic Interventions

The discovery of CRG4 as a potential drug target and biomarker for Down syndrome has led to a great deal of interest in the development of therapeutic interventions. Several potential therapeutic approaches have been proposed to target CRG4 and improve the treatment of Down syndrome.

1. Drug Treatments: One of the most promising therapeutic approaches is the use of drugs that target CRG4. Currently, there are several drug candidates that are being evaluated for their potential to treat Down syndrome. These drugs include atogepant, a sodium channel blocker, and gabapentin, an inhibitor of the nervous system. Other drugs that may be considered for treatment of Down syndrome in the future include hypnotics, antipsychotics, and antiepileptic drugs.

2. Biomarkers: Another approach to treating Down syndrome is the use of biomarkers. Biomarkers are substances that are derived from the body and can be used as indicators of the presence or absence of a particular disease. The development of biomarkers for Down syndrome could lead to the development of non-invasive diagnostic tests and more targeted therapies.

Conclusion

DSCR4 is a gene that has significant implications for the treatment of Down syndrome. Its expression in individuals with Down syndrome suggests that it may be involved in the pathophysiology of this disorder. The discovery of CRG4 as a potential drug target and biomarker for Down syndrome has led to a great deal of interest in the development of therapeutic interventions. Further research is needed to fully understand the role of CRG4 in the development and progression of Down syndrome, and to develop effective treatments.

Protein Name: Down Syndrome Critical Region 4

The "DSCR4 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 DSCR4 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

DSCR8 | DSCR9 | DSE | DSEL | DSEL-AS1 | DSG1 | DSG1-AS1 | DSG2 | DSG3 | DSG4 | DSN1 | DSP | DSP-AS1 | DSPP | DST | DST-AS1 | DSTN | DSTNP2 | DSTYK | DTD1 | DTD1-AS1 | DTD2 | DTHD1 | DTL | DTNA | DTNB | DTNB-AS1 | DTNBP1 | DTWD1 | DTWD2 | DTX1 | DTX2 | DTX2P1 | DTX2P1-UPK3BP1-PMS2P11 | DTX3 | DTX3L | DTX4 | DTYMK | Dual Specificity Mitogen-Activated Protein Kinase Kinase (MEK) | Dual specificity protein kinase (CLK) | Dual specificity protein tyrosine phosphatase | Dual-Specificity Tyrosine-(Y)-Phosphorylation Regulated Kinase 1 | DUBR | DUOX1 | DUOX2 | DUOXA1 | DUOXA2 | DUS1L | DUS2 | DUS3L | DUS4L | DUSP1 | DUSP10 | DUSP11 | DUSP12 | DUSP13 | DUSP14 | DUSP15 | DUSP16 | DUSP18 | DUSP19 | DUSP2 | DUSP21 | DUSP22 | DUSP23 | DUSP26 | DUSP28 | DUSP29 | DUSP3 | DUSP4 | DUSP5 | DUSP5P1 | DUSP6 | DUSP7 | DUSP8 | DUSP8P5 | DUSP9 | DUT | DUTP6 | DUX1 | DUX3 | DUX4 | DUX4L1 | DUX4L13 | DUX4L16 | DUX4L18 | DUX4L19 | DUX4L2 | DUX4L20 | DUX4L23 | DUX4L3 | DUX4L37 | DUX4L4 | DUX4L5 | DUX4L6 | DUX4L7 | DUX4L8 | DUX4L9 | DUXA | DUXAP10