CEP85L centrosomal protein 85 like
Gene ID: 387119, updated on 2-Nov-2024Gene type: protein coding
Also known as: LIS10; C6orf204; NY-BR-15; bA57K17.2
- See all available tests in GTR for this gene
- Go to complete Gene record for CEP85L
- Go to Variation Viewer for CEP85L variants
Summary
The protein encoded by this gene was identified as a breast cancer antigen. Nothing more is known of its function at this time. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23. GeneReviews: Not available | |
| Common variants at ten loci influence QT interval duration in the QTGEN Study. GeneReviews: Not available | |
| Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. GeneReviews: Not available | |
| Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk. GeneReviews: Not available | |
| Impact of ancestry and common genetic variants on QT interval in African Americans. GeneReviews: Not available | |
| Lissencephaly 10 | See labs |
Genomic context
- Location:
- 6q22.31
- Sequence:
- Chromosome: 6; NC_000006.12 (118460772..118710089, complement)
- Total number of exons:
- 21
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for CEP85L variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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