CLRN3 clarin 3
Gene ID: 119467, updated on 2-Nov-2024Gene type: protein coding
Also known as: TMEM12; USH3AL1
- See all available tests in GTR for this gene
- Go to complete Gene record for CLRN3
- Go to Variation Viewer for CLRN3 variants
Summary
Predicted to be involved in sensory perception of sound. Located in extracellular exosome. [provided by Alliance of Genome Resources, Nov 2024]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Genomic determinants of motor and cognitive outcomes in Parkinson's disease. GeneReviews: Not available |
Genomic context
- Location:
- 10q26.2
- Sequence:
- Chromosome: 10; NC_000010.11 (127877841..127892941, complement)
- Total number of exons:
- 3
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for CLRN3 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
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