COX16 cytochrome c oxidase assembly factor COX16
Gene ID: 51241, updated on 11-Apr-2024Gene type: protein coding
Also known as: hCOX16; HSPC203; MC4DN22; C14orf112
- See all available tests in GTR for this gene
- Go to complete Gene record for COX16
- Go to Variation Viewer for COX16 variants
Summary
Involved in mitochondrial cytochrome c oxidase assembly. Is integral component of mitochondrial inner membrane. [provided by Alliance of Genome Resources, Apr 2022]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Mitochondrial complex IV deficiency, nuclear type 22 | not available |
Genomic context
- Location:
- 14q24.2
- Sequence:
- Chromosome: 14; NC_000014.9 (70325081..70359683, complement)
- Total number of exons:
- 4
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for COX16 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
- Variation ViewerRelated Variants
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