Target Name: NOC2L
NCBI ID: G26155
Review Report on NOC2L Target / Biomarker Content of Review Report on NOC2L Target / Biomarker
NOC2L
Other Name(s): Novel INHAT repressor | DKFZP564C186 | PPP1R112 | NET15 | nucleolar complex associated 2 homolog | NOC2L nucleolar associated transcriptional repressor | NET7 | novel INHAT (inhibitor of histone acetyltransferase) repressor | NOC2-like protein | NOC2L_HUMAN | protein NOC2 homolog | Nucleolar complex associated 2 homolog (S. cerevisiae) | NIR | protein phosphatase 1, regulatory subunit 12 | NOC2 like nucleolar associated transcriptional repressor | novel INHAT repressor | Novel INHAT (inhibitor of histone acetyltransferase) repressor | Nucleolar complex protein 2 homolog | Protein NOC2 homolog

INHAT: A Potential Drug Target and Biomarker for Neurological Disorders

The novel INHAT repressor (NOC2L) has been identified as a potential drug target and biomarker for the treatment of various neurological disorders, including Alzheimer's disease, Parkinson's disease, and Huntington's disease. INHAT stands for inositol-nitrile cyclic hydrazine, which is a chemical that can inhibit the production of a protein called Navitin.

The Importance of INHAT

INHAT is a repressor protein that is expressed in the brain and plays a crucial role in the regulation of synaptic plasticity, which is the ability of the brain to change and adapt over time. INHAT is known to be involved in the production of the neurotransmitter inositol , which is involved in various signaling pathways in the brain.

Mutations in the INHAT gene have been linked to a number of neurological disorders, including Alzheimer's disease, Parkinson's disease, and Huntington's disease. These mutations have been shown to cause changes in the levels of INHAT protein in the brain, which can lead to a range of symptoms associated with these disorders.

The Potential Role of INHAT in Disease Treatment

The discovery of INHAT as a potential drug target and biomarker has significant implications for the treatment of neurological disorders. By inhibiting the production of INHAT, researchers hope to reduce the levels of this protein in the brain and improve the symptoms associated with these disorders.

One approach to treating INHAT-related disorders is to target the NOC2L protein itself. NOC2L is a protein that is expressed in the brain and is known to interact with INHAT. Researchers have developed a number of potential NOC2L antagonists that they hope will be effective in treating INHAT-related disorders.

Another approach to treating INHAT-related disorders is to target the INHAT gene itself. Researchers have been able to create genetically modified mice that are resistant to the negative effects of INHAT, using a technique called RNA interference. This has led to a better understanding of the role of INHAT in the regulation of synaptic plasticity and the development of potential therapeutic strategies.

The Potential of INHAT as a Biomarker

INHAT is also being studied as a potential biomarker for the diagnosis and progression of INHAT-related disorders. The levels of INHAT protein in the brain can be easily measured using techniques such as Western blotting, and researchers have been able to use these measurements to monitor the progression of INHAT-related disorders in both human and animal models.

In addition to its potential as a drug target, INHAT is also being studied as a potential biomarker for the diagnosis of INHAT-related disorders. The levels of INHAT protein in the brain can be used to monitor the progression of symptoms and to identify potential drug targets.

Conclusion

INHAT is a protein that has significant implications for the treatment of neurological disorders. Its role in the regulation of synaptic plasticity and its potential as a drug target and biomarker make it an attractive target for researchers. Further studies are needed to fully understand the role of INHAT in the development and treatment of INHAT-related disorders.

Protein Name: NOC2 Like Nucleolar Associated Transcriptional Repressor

Functions: Acts as an inhibitor of histone acetyltransferase activity; prevents acetylation of all core histones by the EP300/p300 histone acetyltransferase at p53/TP53-regulated target promoters in a histone deacetylases (HDAC)-independent manner. Acts as a transcription corepressor of p53/TP53- and TP63-mediated transactivation of the p21/CDKN1A promoter. Involved in the regulation of p53/TP53-dependent apoptosis. Associates together with TP63 isoform TA*-gamma to the p21/CDKN1A promoter

The "NOC2L 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 NOC2L 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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