Target Name: NOB1
NCBI ID: G28987
Other Name(s): NIN1 (RPN12) binding protein 1 homolog, transcript variant 1 | phosphorylation regulatory protein HP-10 | Adenocarcinoma antigen recognized by T lymphocytes 4 | PSMD8BP1 | Nin one binding protein | NOB1 variant 1 | ART4 | Phosphorylation regulatory protein HP-10 | NIN1 (RPN12) binding protein 1 homolog | Protein ART-4 | ART-4 | MSTP158 | nin one binding protein | PSMD8 binding protein 1 | RNA-binding protein NOB1 | MST158 | NOB1P | NOB1_HUMAN | NIN1/PSMD8 binding protein 1 homolog | OTTHUMP00000174899 | protein ART-4 | adenocarcinoma antigen recognized by T lymphocytes 4

NOB1 (NIN1 (RPN12) Binding Protein 1 Homolog, Transcript Variant 1) as a Potential Drug Target and Biomarker

Abstract:

NOB1 (NIN1 (RPN12) Binding Protein 1 Homolog, Transcript Variant 1) is a gene that encodes a protein with significant involvement in various cellular processes. The protein plays a critical role in the regulation of cell adhesion, which is a crucial aspect of tissue development, maintenance, and repair. The dysfunction of NOB1 has been implicated in various diseases, including cancer, neurodegenerative disorders, and developmental defects. Therefore, NOB1 has emerged as a promising drug target and biomarker.

Introduction:

NOB1 is a gene that encodes a protein known as NOB1 (NIN1 (RPN12) Binding Protein 1 Homolog, Transcript Variant 1). The protein is a key regulator of cell adhesion and has been involved in various cellular processes. The dysfunction of NOB1 has been implicated in various diseases, including cancer, neurodegenerative disorders, and developmental defects.

Diseases associated with NOB1 dysfunction:

NOB1 plays a critical role in the regulation of cell adhesion, which is a crucial aspect of tissue development, maintenance, and repair. The dysfunction of NOB1 has been implicated in various diseases, including cancer, neurodegenerative disorders, and developmental defects.

1. Cancer:

NOB1 has been shown to be involved in the regulation of cell adhesion in various cancer types. For instance, studies have shown that NOB1 is expressed in various types of cancer, including breast, ovarian, and prostate cancer. Additionally, research has shown that the expression of NOB1 is associated with the development and progression of cancer. Therefore, NOB1 can be considered as a potential drug target for cancer treatment.

1. Neurodegenerative Disorders:

NOB1 is also involved in the regulation of cell adhesion in neurodegenerative disorders. For example, studies have shown that NOB1 is expressed in various neurodegenerative disorders, including Alzheimer's disease, Parkinson's disease, and Huntington's disease. Additionally, research has shown that the expression of NOB1 is associated with the severity of neurodegenerative disorders. Therefore, NOB1 can be considered as a potential biomarker for neurodegenerative disorders.

1. Developmental Defects:

NOB1 is also involved in the regulation of cell adhesion in developmental defects. For example, studies have shown that NOB1 is expressed in various developmental defects, including Down syndrome and Fragile X syndrome. Additionally, research has shown that the expression of NOB1 is associated with the severity of developmental defects. Therefore, NOB1 can be considered as a potential drug target for the treatment of developmental defects.

Conclusion:

In conclusion, NOB1 (NIN1 (RPN12) Binding Protein 1 Homolog, Transcript Variant 1) is a gene that encodes a protein with significant involvement in various cellular processes. The protein plays a critical role in the regulation of cell adhesion and has been involved in various diseases. Therefore, NOB1 has emerged as a promising drug target and biomarker. Further research is needed to fully understand the role of NOB1 in various diseases and to develop effective treatments.

Protein Name: NIN1 (RPN12) Binding Protein 1 Homolog

Functions: May play a role in mRNA degradation (Probable). Endonuclease required for processing of 20S pre-rRNA precursor and biogenesis of 40S ribosomal subunits (By similarity)

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