Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 7401
MIM: 606397
HGNC: 12605
Ensembl: ENSG00000163646
Variants:
dbSNP: 7401
ClinVar: 7401
TCGA: ENSG00000163646
COSMIC: CLRN1
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35481838 | 2022 | Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort. | 0 |
| 35481838 | 2022 | Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort. | 0 |
| 31968401 | 2020 | Extending the spectrum of CLRN1- and ABCA4-associated inherited retinal dystrophies caused by novel and recurrent variants using exome sequencing. | 4 |
| 31968401 | 2020 | Extending the spectrum of CLRN1- and ABCA4-associated inherited retinal dystrophies caused by novel and recurrent variants using exome sequencing. | 4 |
| 31097578 | 2019 | Unconventional secretory pathway activation restores hair cell mechanotransduction in an USH3A model. | 3 |
| 31097578 | 2019 | Unconventional secretory pathway activation restores hair cell mechanotransduction in an USH3A model. | 3 |
| 29490346 | 2018 | The Genetics of Usher Syndrome in the Israeli and Palestinian Populations. | 7 |
| 29490346 | 2018 | The Genetics of Usher Syndrome in the Israeli and Palestinian Populations. | 7 |
| 28469144 | 2017 | A deep intronic CLRN1 (USH3A) founder mutation generates an aberrant exon and underlies severe Usher syndrome on the Arabian Peninsula. | 20 |
| 28469144 | 2017 | A deep intronic CLRN1 (USH3A) founder mutation generates an aberrant exon and underlies severe Usher syndrome on the Arabian Peninsula. | 20 |
| 25743179 | 2015 | Identification of a novel CLRN1 gene mutation in Usher syndrome type 3: two case reports. | 1 |
| 25743179 | 2015 | Identification of a novel CLRN1 gene mutation in Usher syndrome type 3: two case reports. | 1 |
| 22681893 | 2013 | Extended mutation spectrum of Usher syndrome in Finland. | 6 |
| 22964989 | 2013 | Cone structure in patients with usher syndrome type III and mutations in the Clarin 1 gene. | 24 |
| 22681893 | 2013 | Extended mutation spectrum of Usher syndrome in Finland. | 6 |
Citation
Dessen P
CLRN1 (clarin 1)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/61903/clrn1-(clarin-1)
