NOP16 NOP16 nucleolar protein
Gene ID: 51491, updated on 17-Sep-2024Gene type: protein coding
Also known as: HSPC111; HSPC185
- See all available tests in GTR for this gene
- Go to complete Gene record for NOP16
- Go to Variation Viewer for NOP16 variants
Summary
This gene encodes a protein that is localized to the nucleolus. Expression of this gene is induced by estrogens and Myc protein and is a marker of poor patient survival in breast cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]
Genomic context
- Location:
- 5q35.2
- Sequence:
- Chromosome: 5; NC_000005.10 (176383946..176388598, complement)
- Total number of exons:
- 6
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for NOP16 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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