Target Name: SNORD115-11
NCBI ID: G100033448
Review Report on SNORD115-11 Target / Biomarker Content of Review Report on SNORD115-11 Target / Biomarker
Other Name(s): HBII-52-11 | Small nucleolar RNA, C/D box 115-11 | small nucleolar RNA, C/D box 115-11

The Importance of SNORD115-11 as a Potential Disease Drug Target or Biomarker

SNORD115-11 is a small nucleolar RNA (snoRNA) molecule that has gained significant attention in recent years for its potential implications in disease progression. This article aims to explore the role of SNORD115-11 as a potential disease drug target or biomarker, highlighting its significance and potential applications in various medical fields.

Understanding SNORD115-11
SNORD115-11 is a member of the SNORD115 gene cluster located on chromosome 15q11-q13, which is associated with a range of genetic disorders and neurodevelopmental conditions, including Prader-Willi syndrome (PWS) and Angelman syndrome (AS). It is specifically a member of the C/D box snoRNAs family.

Based on its genetic location within the imprinted 15q11-q13 region, SNORD115-11 is exclusively expressed from the paternal allele, often in the brain's neurons. This specific pattern of expression suggests its potential involvement in various neurological processes and its association with neurodevelopmental disorders.

SNORD115-11 as a Disease Drug Target
The unique expression pattern of SNORD115-11 and its association with neurological disorders make it an attractive target for potential therapeutic interventions. Understanding the molecular mechanisms of SNORD115-11 can provide valuable insights into the underlying causes of these disorders and potentially lead to the development of new treatment strategies.

PWS, for example, is characterized by central hypotonia, infantile feeding difficulties, and subsequent hyperphagia leading to obesity. The absence or disruption of the SNORD115 gene cluster has been linked to the PWS phenotype. Therefore, identifying specific drug targets within this cluster, including SNORD115-11, may offer novel therapeutic avenues to manage symptoms and improve the quality of life for PWS patients.

Similarly, AS, a neurodevelopmental disorder characterized by severe intellectual disability and neurological abnormalities, is also associated with abnormalities in the SNORD115 gene cluster. As such, targeting SNORD115-11 may hold promise for the development of AS-specific therapies aimed at ameliorating the cognitive and neurological symptoms associated with the condition.

The discovery and characterization of SNORD115-11 as a disease-specific drug target may pave the way for personalized medicine, allowing for tailored treatments depending on the patient's specific genetic makeup and neurological phenotype.

SNORD115-11 as a Potential Biomarker
In addition to its potential as a therapeutic target, SNORD115-11 also holds promise as a biomarker for various diseases. A biomarker is a measurable indicator that can be used to diagnose a disease, predict its progression, or evaluate the effectiveness of a therapeutic intervention. SNORD115-11's distinct expression pattern and association with specific disorders make it a potential biomarker candidate.

For instance, the levels of SNORD115-11 expression in the brain could potentially serve as a diagnostic tool for PWS and AS, aiding in early detection and individualized treatment plans. Similarly, monitoring the expression levels of SNORD115-11 in peripheral tissues may enable the development of non-invasive diagnostic tests for these disorders.

Furthermore, SNORD115-11 could potentially serve as a biomarker for other neurological conditions beyond PWS and AS. By studying its expression levels across various brain disorders, researchers may uncover common underlying mechanisms or specific patterns associated with different conditions, aiding in accurate diagnoses and more focused treatment strategies.

SNORD115-11, a small nucleolar RNA molecule located on the 15q11-q13 chromosome region, holds significant potential as a disease drug target or biomarker. Its unique expression patterns in the brain, particularly in neurodevelopmental disorders such as PWS and AS, make it an attractive candidate for therapeutic interventions. Additionally, its distinct expression patterns offer opportunities for using SNORD115-11 as a biomarker for accurate diagnosis and evaluation of disease progression in various neurological conditions. Ongoing research focused on understanding the molecular functions and interactions of SNORD115-11 may uncover novel therapeutic strategies and diagnostic tools with the potential to revolutionize personalized medicine in the future.

Protein Name: Small Nucleolar RNA, C/D Box 115-11

The "SNORD115-11 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 SNORD115-11 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

More Common Targets

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