CWC15 CWC15 spliceosome associated protein homolog
Gene ID: 51503, updated on 3-Nov-2024Gene type: protein coding
Also known as: ORF5; AD002; Cwf15; C11orf5; HSPC148
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- Go to complete Gene record for CWC15
- Go to Variation Viewer for CWC15 variants
Summary
Predicted to enable RNA binding activity. Involved in mRNA splicing, via spliceosome. Located in mitochondrion and nuclear speck. Part of Prp19 complex and U2-type catalytic step 2 spliceosome. [provided by Alliance of Genome Resources, Nov 2024]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. GeneReviews: Not available |
Genomic context
- Location:
- 11q21
- Sequence:
- Chromosome: 11; NC_000011.10 (94962620..94973556, complement)
- Total number of exons:
- 7
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for CWC15 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
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