Rpl11 Gene plays an important role in the study of neurodegenerative diseases. This page provides comprehensive information about this topic, including its mechanisms, significance in disease processes, and therapeutic implications.
Rpl11 Gene is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.
RPL11 (Ribosomal Protein L11) is a gene encoding a ribosomal protein that is a component of the 60S ribosomal subunit.
| Attribute | Value |
|---|---|
| Gene Symbol | RPL11 |
| Full Name | Ribosomal Protein L11 |
| Chromosomal Location | 1p36.1 |
| NCBI Gene ID | 6135 |
| OMIM | 604175 |
| Ensembl ID | ENSG00000142676 |
| UniProt ID | P62913 |
RPL11 is a ribosomal protein component of the 60S large ribosomal subunit. It is involved in:
Mutations in RPL11 cause:
Rpl11 Gene plays an important role in the study of neurodegenerative diseases. This page provides comprehensive information about this topic, including its mechanisms, significance in disease processes, and therapeutic implications.
The study of Rpl11 Gene has evolved significantly over the past decades. Research in this area has revealed important insights into the underlying mechanisms of neurodegeneration and continues to drive therapeutic development.
Historical context and key discoveries in this field have shaped our current understanding and will continue to guide future research directions.
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