UQCC3 ubiquinol-cytochrome c reductase complex assembly factor 3
Gene ID: 790955, updated on 3-Nov-2024Gene type: protein coding
Also known as: MC3DN9; UNQ655; C11orf83; CCDS41658.1
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- Go to complete Gene record for UQCC3
- Go to Variation Viewer for UQCC3 variants
Summary
Complex III is a mitochondrial inner membrane protein complex that transfers electrons from ubiquinol to cytochrome c. This gene encodes a protein that functions in complex III assembly. Mutations in this gene result in Mitochondrial complex III deficiency, nuclear type 9. [provided by RefSeq, Dec 2014]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Mitochondrial complex III deficiency nuclear type 9 | See labs |
Genomic context
- Location:
- 11q12.3
- Sequence:
- Chromosome: 11; NC_000011.10 (62671673..62673686)
- Total number of exons:
- 2
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for UQCC3 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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