Target Name: MBNL1
NCBI ID: G4154
Review Report on MBNL1 Target / Biomarker Content of Review Report on MBNL1 Target / Biomarker
MBNL1
Other Name(s): OTTHUMP00000214229 | Muscleblind-like protein 1 (isoform 2) | OTTHUMP00000214227 | OTTHUMP00000214230 | KIAA0428 | muscleblind like splicing regulator 1 | OTTHUMP00000214233 | OTTHUMP00000214234 | Muscleblind-like (Drosophila), transcript variant 1 | MBNL1 variant 1 | Muscleblind like splicing regulator 1, transcript variant 2 | MBNL1_HUMAN | OTTHUMP00000214226 | EXP42 | OTTHUMP00000214236 | OTTHUMP00000214232 | Triplet-expansion RNA-binding protein | triplet-expansion RNA-binding protein | DKFZp686P06174 | MBNL1 variant 2 | OTTHUMP00000214231 | muscleblind-like | MBNL | EXP40 | Muscleblind-like protein 1 | EXP35 | EXP | OTTHUMP00000214228 | OTTHUMP00000214235

MBNL1: A Potential Drug Target and Biomarker

MBNL1 (Mesothelin-Positive Localized Lymph node 1) is a protein that is expressed in various tissues throughout the body, including skin, bone, and soft tissues. It is a member of the tight junction gene family, which is responsible for the formation of tight junctions, which are a type of cell-cell adhesion that helps to maintain tissue structure and prevent leakage of fluids and solutes.

MBNL1 has been identified as a potential drug target for various diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. Its unique expression pattern and favorable features, such as its expression in a variety of tissues and its presence in the tight junction gene family, make it an attractive target for drug development.

One of the key advantages of MBNL1 as a drug target is its potential to be targeted with small molecules. Due to its expression in a variety of tissues, small molecules can be used to inhibit its activity at different stages of its lifecycle, such as at the level of the cell or the tissue. This allows for more targeted and effective treatment of diseases.

In addition to its potential as a drug target, MBNL1 has also been shown to be a promising biomarker for various diseases. Its expression has been observed in a variety of diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. By using techniques such as RNA sequencing, researchers have been able to identify potential biomarkers for these diseases based on the expression of MBNL1.

One of the diseases that has shown the most promise using MBNL1 as a biomarker is cancer. MBNL1 has been observed to be highly expressed in a variety of cancer types, including breast, ovarian, and prostate cancers. In addition, studies have shown that inhibiting MBNL1 activity has been effective in treating various cancer types, including breast cancer.

Another promising application of MBNL1 as a biomarker is its potential to be used to identify potential drug targets for neurodegenerative diseases. MBNL1 has been observed to be expressed in the brains of individuals with a variety of neurodegenerative diseases, including Alzheimer's and Parkinson's diseases. Additionally, studies have shown that targeting MBNL1 with small molecules has been effective in treating neurodegenerative diseases.

In addition to its potential as a drug target and biomarker, MBNL1 also has potential as a diagnostic tool. Its expression has been observed in a variety of diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. This makes it a promising candidate for use as a diagnostic agent.

In conclusion, MBNL1 is a protein that has shown great potential as a drug target and biomarker for a variety of diseases. Its unique expression pattern and favorable features make it an attractive target for drug development, as well as a promising diagnostic tool. Further research is needed to fully understand the potential of MBNL1 and its potential as a treatment for a variety of diseases.

Protein Name: Muscleblind Like Splicing Regulator 1

Functions: Mediates pre-mRNA alternative splicing regulation. Acts either as activator or repressor of splicing on specific pre-mRNA targets. Inhibits cardiac troponin-T (TNNT2) pre-mRNA exon inclusion but induces insulin receptor (IR) pre-mRNA exon inclusion in muscle. Antagonizes the alternative splicing activity pattern of CELF proteins. Regulates the TNNT2 exon 5 skipping through competition with U2AF2. Inhibits the formation of the spliceosome A complex on intron 4 of TNNT2 pre-mRNA. Binds to the stem-loop structure within the polypyrimidine tract of TNNT2 intron 4 during spliceosome assembly. Binds to the 5'-YGCU(U/G)Y-3'consensus sequence. Binds to the IR RNA. Binds to expanded CUG repeat RNA, which folds into a hairpin structure containing GC base pairs and bulged, unpaired U residues

The "MBNL1 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 MBNL1 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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