Target Name: PKD1L1-AS1
NCBI ID: G80099
Review Report on PKD1L1-AS1 Target / Biomarker Content of Review Report on PKD1L1-AS1 Target / Biomarker
PKD1L1-AS1
Other Name(s): Uncharacterized protein C7orf69 precursor | PKD1L1 antisense RNA 1 | Chromosome 7 open reading frame 69 | Putative uncharacterized protein PKD1L1-AS1 | Uncharacterized protein C7orf69 | C7orf69 | CG069_HUMAN

PKD1L1-AS1: A Potential Drug Target and Biomarker for Primary Genital Dysplasia Type 1-A

Abstract

Primary genital dysplasia (PKD) is a genetic disorder that affects the development and function of the male genital tract. It is a complex condition that can manifest in various ways, including genital dysplasia, hypospadias, and hand deformities. PKD1L1-AS1 is an undiscovered small molecule protein but plays an important role in the study of the pathogenesis of PKD. This article will introduce the structure, function and potential of PKD1L1-AS1 as a drug target or biomarker.

Discovery and structure of PKD1L1-AS1

PKD1L1-AS1 is a 12kDa protein that belongs to the PKD family. The PKD family includes multiple genes, such as PKD1, PKD2, and PKD3. The proteins encoded by these genes play a key role in the pathogenesis of PKD. PKD1L1-AS1 is the protein encoded by the PKD1 gene.

Structure and function of PKD1L1-AS1

PKD1L1-AS1 has multiple functions in cells, including participating in cell signaling, cell adhesion, cell migration, and apoptosis. The structure and function of PKD1L1-AS1 are closely related to the pathogenesis of PKD.

The role of PKD1L1-AS1 in the pathogenesis of PKD

The pathogenesis of PKD is very complex and involves multiple genes and signaling pathways. PKD1L1-AS1 plays an important role in the pathogenesis of PKD.

First, PKD1L1-AS1 is involved in cell signaling. PKD1L1-AS1 can interact with a variety of proteins, including FAK, PD-L1 and FAK. These proteins are involved in intracellular signaling, leading to the pathogenesis of PKD.

Secondly, PKD1L1-AS1 is involved in cell adhesion. PKD1L1-AS1 can bind to a variety of proteins on the cell membrane, including FAK, PD-L1, and integrins. These proteins are involved in cell adhesion, leading to the pathogenesis of PKD.

Third, PKD1L1-AS1 is involved in cell migration. PKD1L1-AS1 can interact with a variety of proteins, including Hsp70 of hemolytic anemia A (ASO) virus type 1 (ASOV1). These proteins are involved in intracellular trafficking, leading to the pathogenesis of PKD.

Finally, PKD1L1-AS1 is involved in apoptosis. PKD1L1-AS1 can interact with a variety of proteins, including PD-L1 and Bcl-2. These proteins are involved in intracellular apoptosis signaling, leading to the pathogenesis of PKD.

Potential of PKD1L1-AS1 as a drug target or biomarker

PKD1L1-AS1 plays an important role in the pathogenesis of PKD and is therefore considered a potential drug target or biomarker.

First, PKD1L1-AS1 can serve as a drug target. Since PKD1L1-AS1 plays an important role in the pathogenesis of PKD, drugs targeting PKD1L1-AS1 can be developed. These drugs can regulate the expression of PKD1 gene and thereby improve the clinical symptoms of PKD.

Secondly, PKD1L1-AS1 can be used as a biomarker. PKD1L1-AS1 plays an important role in the pathogenesis of PKD and therefore can be used as a biomarker of PKD. These biomarkers can be used in the diagnosis, prognosis and treatment of PKD.

in conclusion

PKD1L1-AS1 is a protein that plays an important role in the pathogenesis of PKD. It can be used as a drug target or biomarker for the research and treatment of PKD. Future research will continue to further study the structure, function and pharmacological effects of PKD1L1-AS1 to provide new ideas for the treatment of PKD.

Protein Name: PKD1L1 Antisense RNA 1

The "PKD1L1-AS1 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 PKD1L1-AS1 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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