Target Name: ASH2L
NCBI ID: G9070
Review Report on ASH2L Target / Biomarker Content of Review Report on ASH2L Target / Biomarker
ASH2L
Other Name(s): Bre2 | Set1/Ash2 histone methyltransferase complex subunit ASH2 (isoform a) | ASH2L1 | ASH2L_HUMAN | ASH2-like protein | Ash2 (absent, small, or homeotic)-like | ASH2L variant 1 | ASH2 like, histone lysine methyltransferase complex subunit, transcript variant 1 | Set1/Ash2 histone methyltransferase complex subunit ASH2 | ASH2 | Ash2-like | ASH2L variant 2 | ASH2L2 | Set1/Ash2 histone methyltransferase complex subunit ASH2 (isoform b) | ASH2 like, histone lysine methyltransferase complex subunit, transcript variant 2 | ASH2 like, histone lysine methyltransferase complex subunit | ash2 (absent, small, or homeotic)-like

ASH2L: A Potential Drug Target and Biomarker for the Treatment of Asperger's Syndrome

Introduction

Asperger's syndrome is a neurodevelopmental disorder that is characterized by difficulties in social interaction, communication, and repetitive behaviors. Despite being diagnosed in millions of individuals worldwide, the understanding of the underlying mechanisms of this disorder remains limited. Recent research has identified several potential drug targets and biomarkers that may have the potential to improve the treatment of asperger's syndrome. In this article, we will focus on one such potential drug target and biomarker, ASH2L, and its potential implications for the treatment of asperger's syndrome.

ASH2L: A Potential Drug Target

ASH2L, also known as break2, is a non-coding RNA molecule that has been identified as a potential drug target for the treatment of asperger's syndrome. ASH2L is expressed in virtually all tissues of the body and has been shown to play a role in the development and maintenance of asperger's syndrome.

Studies have shown that ASH2L is involved in the regulation of various cellular processes, including cell growth, differentiation, and RNA translation. It has also been shown to play a role in the development of neurofibrillary tangles, a hallmark of neurodegenerative diseases, which are observed in individuals with asperger's syndrome.

In addition to its role in neurodegeneration, ASH2L has also been shown to be involved in the regulation of immune and nervous system function. Studies have shown that ASH2L can modulate the immune response and contribute to the development of autoimmune disorders, which are common in individuals with asperger's syndrome.

ASH2L also has been shown to play a role in the regulation of pain perception and neuroinflammation, which are also observed in individuals with asperger's syndrome.

Potential Therapeutic Strategies

The potential therapeutic strategies for ASH2L are vast and include several different approaches. One approach is to target ASH2L directly with small molecules or antibodies to reduce its levels and improve the production of other proteins that are involved in the development and maintenance of asperger's syndrome.

Another approach is to target ASH2L with drugs that can modulate its levels or activity. For example, drugs that can inhibit the activity of ASH2L enzymes or modulate its stability could be used to reduce its levels and improve the production of other proteins.

Another approach is to target ASH2L with drugs that can modulate its interactions with other proteins. For example, drugs that can bind to ASH2L and modulate its interactions with other proteins could be used to reduce its levels and improve the production of other proteins.

Another approach is to target ASH2L directly with small molecules or antibodies to reduce its levels and improve the production of other proteins that are involved in the development and maintenance of asperger's syndrome.

Conclusion

In conclusion, ASH2L is a potential drug target and biomarker for the treatment of asperger's syndrome. Its role in the regulation of various cellular processes and its involvement in the development and maintenance of asperger's syndrome make it an attractive target for therapeutic intervention. Further research is needed to fully understand the potential therapeutic strategies for ASH2L and to develop safe and effective treatments for asperger's syndrome.

Protein Name: ASH2 Like, Histone Lysine Methyltransferase Complex Subunit

Functions: Transcriptional regulator (PubMed:12670868). Component or associated component of some histone methyltransferase complexes which regulates transcription through recruitment of those complexes to gene promoters (PubMed:19131338). Component of the Set1/Ash2 histone methyltransferase (HMT) complex, a complex that specifically methylates 'Lys-4' of histone H3, but not if the neighboring 'Lys-9' residue is already methylated (PubMed:19556245). As part of the MLL1/MLL complex it is involved in methylation and dimethylation at 'Lys-4' of histone H3 (PubMed:19556245). May play a role in hematopoiesis (PubMed:12670868). In association with RBBP5 and WDR5, stimulates the histone methyltransferase activities of KMT2A, KMT2B, KMT2C, KMT2D, SETD1A and SETD1B (PubMed:21220120, PubMed:22266653)

The "ASH2L 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 ASH2L 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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