Target Name: RAD21L1
NCBI ID: G642636
Review Report on RAD21L1 Target / Biomarker Content of Review Report on RAD21L1 Target / Biomarker
RAD21L1
Other Name(s): RAD21L | Double-strand-break repair protein rad21-like protein 1 | dJ545L17.2 | Double-strand-break repair protein rad21-like protein 1 (isoform 1) | RAD21 cohesin complex component like 1 | RAD21 cohesin complex component like 1, transcript variant 1 | RAD21-like 1 | RAD21L1 variant 1 | RD21L_HUMAN

RAD21L1: A Potential Drug Target for Diseases

RAD21L1 is a gene that encodes a protein known as RAD21, which is a key regulator of the DNA damage response pathway. Mutations in the RAD21 gene have been linked to a variety of diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. As a As a result, RAD21L1 has emerged as a promising drug target for a variety of diseases.

The DNA damage response pathway is a critical regulatory process that helps cells respond to DNA damage, including mutations, virus infections, and radiation exposure. The pathway involves a series of complex enzymes that detect DNA damage and respond to it. undergo repair or apoptosis. RAD21 is a key regulator in the DNA damage response pathway. The protein RAD21 encoded by the RAD21L1 gene plays a key role in the DNA damage response pathway.

Effects of RAD21L1 gene mutations

RAD21 gene mutations will lead to changes in RAD21 protein expression and function, thereby affecting the DNA damage response pathway. RAD21 gene mutations can lead to changes in the conformation of RAD21 protein, thereby affecting its function. Some studies have shown that RAD21 gene mutations can lead to reduced enzyme activity in the DNA damage response pathway, resulting in DNA damage that cannot be repaired in time, thereby increasing the risk of disease.

The relationship between RAD21L1 and cancer

RAD21L1 gene mutations are closely related to the occurrence and development of various cancers. For example, studies have found that RAD21 gene mutations are closely related to the onset and development of colon cancer, liver cancer, breast cancer and other cancers. In addition, RAD21 gene mutations are closely related to tumor cell metastasis and treatment resistance. Therefore, RAD21L1 is considered a potential tumor therapeutic target.

The relationship between RAD21L1 and neurodegenerative diseases

RAD21L1 gene mutations are closely related to the occurrence and development of neurodegenerative diseases. For example, studies have found that RAD21 gene mutations are closely related to the occurrence and development of various neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease. In addition, RAD21 gene mutations are closely related to the survival rate and quality of life of patients with neurodegenerative diseases. Therefore, RAD21L1 is considered a potential therapeutic target for neurodegenerative diseases.

The relationship between RAD21L1 and immune diseases

RAD21L1 gene mutations are closely related to the occurrence and development of immune diseases. For example, studies have found that RAD21 gene mutations are closely related to the occurrence and development of various immune diseases such as autoimmune diseases and inflammatory bowel disease. In addition, RAD21 gene mutations are also closely related to the risk of immune diseases and disease severity. Therefore, RAD21L1 is considered a potential therapeutic target for immune diseases.

Therapeutic prospects of RAD21L1

With the in-depth research on the association between RAD21L1 gene mutations and the occurrence and development of diseases, RAD21L1 has been considered as a potential drug target. Currently, there are many studies devoted to developing RAD21L1-targeted therapeutic drugs to treat various diseases. For example, some studies are exploring the use of anti-RAD21L1 antibody drugs to treat cancer, neurodegenerative diseases, and immune diseases. In addition, some studies are exploring the use of RNA interference technology to regulate the expression of RAD21L1 gene to treat diseases.

in conclusion

The protein RAD21 encoded by the RAD21L1 gene plays a key role in the DNA damage response pathway. RAD21L1 gene mutations will lead to changes in RAD21 protein expression and function, thereby affecting the DNA damage response pathway. RAD21L1 is closely related to the occurrence and development of many diseases, including cancer, neurodegenerative diseases, and immune diseases. Therefore, RAD21L1 is considered a potential drug target, and many studies have been devoted to developing RAD21L1-targeted therapeutic drugs to treat various diseases.

Protein Name: RAD21 Cohesin Complex Component Like 1

Functions: Meiosis-specific component of some cohesin complex required during the initial steps of prophase I in male meiosis. Probably required during early meiosis in males for separation of sister chromatids and homologous chromosomes. Replaces RAD21 in premeiotic S phase (during early stages of prophase I), while RAD21 reappears in later stages of prophase I. Involved in synaptonemal complex assembly, synapsis initiation and crossover recombination between homologous chromosomes during prophase I (By similarity)

The "RAD21L1 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 RAD21L1 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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