| CLRN1 — Clarin 1 | |
|---|---|
| Symbol | CLRN1 |
| Full Name | Clarin 1 |
| Chromosome | 3q25.31 |
| NCBI Gene | 79568 |
| Ensembl | ENSG00000163631 |
| OMIM | 605792 |
| UniProt | Q9NYQ5 |
| Diseases | Usher Syndrome |
| Expression | Retina, Cochlea |
| Key Mutations | |
| N48K mutation | |
Clrn1 — Clarin 1 is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.
CLRN1 (Clarin 1) is a gene located on chromosome 3q25.31 that plays a critical role in neurodegenerative disease. Mutations in CLRN1 are associated with Usher Syndrome. The gene is catalogued as NCBI Gene ID 79568 and OMIM 605792.
The CLRN1 gene encodes a protein that is expressed in multiple brain regions including Retina, Cochlea. The normal function of this gene product is essential for neuronal health and survival.
Expression data is available from the Allen Human Brain Atlas.
CLRN1 mutations are linked to the following neurodegenerative conditions:
Publication list pending enrichment from PubMed.
The study of Clrn1 — Clarin 1 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.
Page auto-generated from NeuroWiki gene database. Last updated: 2026-02-26.