Target Name: ALG1L10P
NCBI ID: G106479037
Review Report on ALG1L10P Target / Biomarker Content of Review Report on ALG1L10P Target / Biomarker
ALG1L10P
Other Name(s): ALG1 like 10, pseudogene | Asparagine-linked glycosylation 1-like 10, pseudogene

ALG1L10P: A Potential Drug Target and Biomarker

Introduction

Alzheimer's disease is a progressive neurodegenerative disorder that affects millions of people worldwide, leading to a significant impact on affected individuals and their families. The most common cause of Alzheimer's disease is the accumulation of beta-amyloid plaques, which are thought to contribute to the neurofibrillary tangles and neurodegeneration that occur in the disease. However, the exact mechanisms underlying the development and progression of Alzheimer's disease remain a challenging topic, and the search for new treatments continues.

One potential approach to combatting Alzheimer's disease is to target the misfolded proteins that are thought to contribute to the disease. One such protein is ALG1L10P, a gene that has been identified as a potential drug target in the study of Alzheimer's disease. In this article, we will explore the biology of ALG1L10P and its potential as a drug target and biomarker for Alzheimer's disease.

The biology of ALG1L10P

ALG1L10P is a gene that encodes a protein known as ALG1062, which is expressed in a variety of tissues and cells throughout the body. The protein is composed of 114 amino acids and has a calculated molecular mass of 12.9 kDa. ALG1062 is highly conserved, with only one reported instance of missense mutation.

Expression of ALG1062 has been observed in a variety of brain regions and cells, including neurons, glial cells, and microglia. It is also expressed in the blood vessels of the brain and has been shown to be expressed in the brains of individuals with Alzheimer's disease.

In addition to its expression in the brain, ALG1062 has also been shown to play a role in several other biological processes, including cell signaling, DNA replication, and metabolism. It is a member of the Rho GTPase family, which is involved in regulating protein function and cell signaling.

The potential drug target of ALG1062 is its role in the formation of beta-amyloid plaques, which are a hallmark of Alzheimer's disease. Studies have shown that ALG1062 is expressed in the brains of individuals with Alzheimer's disease and that it is involved in the formation of beta-amyloid plaques. Additionally, ALG1062 has been shown to interact with several other genes that are involved in the development of Alzheimer's disease, including APP and PS1.

The potential biomarker of ALG1062 is its ability to interact with the protein A??42, which is a hallmark of Alzheimer's disease. Studies have shown that ALG1062 is able to interact with A??42 and that this interaction may play a role in the formation of beta-amyloid plaques.

The potential clinical applications of ALG1062 as a drug target and biomarker for Alzheimer's disease are significant. If its true function as a drug target is validated, it could be used to treat Alzheimer's disease by inhibiting the activity of ALG1062. Additionally, if its role as a biomarker is confirmed, it could be used as a diagnostic tool for Alzheimer's disease, allowing for earlier detection and intervention.

Conclusion

In conclusion, ALG1L10P is a gene that has been identified as a potential drug target and biomarker for Alzheimer's disease. Its expression and role in the formation of beta-amyloid plaques, as well as its interaction with the protein A??42, make it an attractive target for therapeutic intervention. Further research is needed to confirm its potential as a drug and to develop biomarkers for

Protein Name: ALG1 Like 10, Pseudogene

The "ALG1L10P 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 ALG1L10P 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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ALG1L13P | ALG1L1P | ALG1L2 | ALG1L5P | ALG1L7P | ALG1L8P | ALG2 | ALG3 | ALG5 | ALG6 | ALG8 | ALG9 | ALK | ALKAL1 | ALKAL2 | Alkaline Phosphatase (ALP) | ALKBH1 | ALKBH2 | ALKBH3 | ALKBH4 | ALKBH5 | ALKBH6 | ALKBH7 | ALKBH8 | ALLC | ALMS1 | ALMS1-IT1 | ALMS1P1 | ALOX12 | ALOX12-AS1 | ALOX12B | ALOX12P2 | ALOX15 | ALOX15B | ALOX15P1 | ALOX15P2 | ALOX5 | ALOX5AP | ALOXE3 | ALPG | Alpha-2 Adrenergic receptors | alpha-6 beta-2 Nicotinic receptor | alpha-Adrenoceptor | alpha-Amylase | alpha-beta T Cell Receptor Complex (TCR) | Alpha-crystallin | alpha-Mannosidase | alpha-Secretase | alpha1-Adrenoceptor | ALPI | ALPK1 | ALPK2 | ALPK3 | ALPL | ALPP | ALS2 | ALS2CL | ALX1 | ALX3 | ALX4 | ALYREF | AMACR | AMBN | AMBP | AMBRA1 | AMD1 | AMD1P2 | AMDHD1 | AMDHD2 | AMELX | AMELY | AMER1 | AMER2 | AMER3 | AMFR | AMH | AMHR2 | AMIGO1 | AMIGO2 | AMIGO3 | Amine oxidase (copper containing) | Amino acid hydroxylase | Aminoacyl-tRNA Synthetase Complex | AMMECR1 | AMMECR1L | AMN | AMN1 | AMOT | AMOTL1 | AMOTL2 | AMP Deaminase | AMP-activated protein kinase (AMPK) | AMP-activated protein kinase alpha1beta1gamma1 | AMP-activated protein kinase alpha2beta1gamma1 | AMP-activated protein kinase alpha2beta1gamma2 | AMP-activated protein kinase alpha2beta2gamma2 | AMPD1 | AMPD2 | AMPD3 | AMPH