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: 645104
HGNC: 33939
Ensembl: ENSG00000249581
Variants:
dbSNP: 645104
ClinVar: 645104
TCGA: ENSG00000249581
COSMIC: CLRN2
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000249581 | ENST00000511148 | A0PK11 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33496845 | 2021 | A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans. | 12 |
| 33496845 | 2021 | A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans. | 12 |
| 31448880 | 2019 | Clarin-2 is essential for hearing by maintaining stereocilia integrity and function. | 9 |
| 31448880 | 2019 | Clarin-2 is essential for hearing by maintaining stereocilia integrity and function. | 9 |
Citation
Dessen P
CLRN2 (clarin 2)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/61905/clrn2-(clarin-2)
