Target Name: UBXN2A
NCBI ID: G165324
Review Report on UBXN2A Target / Biomarker Content of Review Report on UBXN2A Target / Biomarker
UBXN2A
Other Name(s): UBX domain-containing protein 2A | UBX domain-containing protein 4 | UBXD4 | UBX domain protein 2A | UBX domain containing 4 | UBX2A_HUMAN

UBXN2A: A Potential Drug Target and Biomarker

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UBXN2A, a gene that encodes a protein known as UBXN2A, has been identified as a potential drug target and biomarker for various neurological and psychiatric disorders. The UBXN2A gene has been shown to play a crucial role in the development and progression of several neurological disorders, including Alzheimer's disease, Parkinson's disease, and epilepsy.

Several studies have demonstrated that UBXN2A is involved in the formation of neurofibrillary tangles, a hallmark of Alzheimer's disease, and that it is associated with increased neurodegeneration in the brain. Additionally, UBXN2A has been shown to regulate the activity of genes involved in the development of epilepsy and other neurological disorders.

As a potential drug target, UBXN2A is being investigated for its ability to treat neurodegenerative disorders. Studies have shown that UBXN2A can be effectively targeted with small molecules, such as RNA interference compounds, to reduce the activity of UBXN2A and prevent neurofibrillary tangles from forming. This approach has the potential to treat a wide range of neurodegenerative disorders, including Alzheimer's disease, Parkinson's disease, and other forms of epilepsy.

In addition to its potential as a drug target, UBXN2A has also been identified as a biomarker for several neurological disorders. The UBXN2A gene has been shown to be significantly altered in individuals with Alzheimer's disease, and these changes have been associated with increased neurodegeneration and decreased lifespan. Similarly, individuals with Parkinson's disease have been shown to have increased levels of UBXN2A in their brains.

These findings suggest that UBXN2A may be a promising biomarker for several neurological disorders, including Alzheimer's disease, Parkinson's disease, and epilepsy. Further research is needed to fully understand the role of UBXN2A in these disorders and to develop effective treatments.

In conclusion, UBXN2A is a gene that has the potential to revolutionize our understanding of the development and progression of neurological disorders. Its involvement in the formation of neurofibrillary tangles and its association with neurodegeneration in the brain make it an attractive drug target for the treatment of neurodegenerative disorders. Additionally, UBXN2A has also been shown to be a biomarker for several neurological disorders, making it an important tool in the search for new treatments. Further research is needed to fully understand the role of UBXN2A in these disorders and to develop effective treatments.

Protein Name: UBX Domain Protein 2A

The "UBXN2A 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 UBXN2A 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

More Common Targets

UBXN2B | UBXN4 | UBXN6 | UBXN7 | UBXN8 | UCA1 | UCHL1 | UCHL1-DT | UCHL3 | UCHL5 | UCK1 | UCK2 | UCKL1 | UCKL1-AS1 | UCMA | UCN | UCN2 | UCN3 | UCP1 | UCP2 | UCP3 | UDP-Glycosyltransferase | UDP-N-Acetylglucosamine--Peptide N-Acetylglucosaminyltransferase (O-GlcNAc Transferase) | UEVLD | UFC1 | UFD1 | UFD1-AS1 | UFL1 | UFM1 | UFSP1 | UFSP2 | UGCG | UGDH | UGDH-AS1 | UGGT1 | UGGT2 | UGP2 | UGT1A1 | UGT1A10 | UGT1A3 | UGT1A4 | UGT1A5 | UGT1A6 | UGT1A7 | UGT1A8 | UGT1A9 | UGT2A1 | UGT2A2 | UGT2A3 | UGT2B10 | UGT2B11 | UGT2B15 | UGT2B17 | UGT2B27P | UGT2B28 | UGT2B29P | UGT2B4 | UGT2B7 | UGT3A1 | UGT3A2 | UGT8 | UHMK1 | UHRF1 | UHRF2 | UICLM | UIMC1 | ULBP1 | ULBP2 | ULBP3 | ULK1 | ULK2 | ULK3 | ULK4 | ULK4P1 | ULK4P2 | ULK4P3 | UMAD1 | UMLILO | UMOD | UMODL1 | UMODL1-AS1 | UMPS | UNC119 | UNC119-myristate complex | UNC119B | UNC13A | UNC13B | UNC13C | UNC13D | UNC45A | UNC45B | UNC50 | UNC5A | UNC5B | UNC5B-AS1 | UNC5C | UNC5CL | UNC5D | UNC79 | UNC80