FMC1 formation of mitochondrial complex V assembly factor 1 homolog
Gene ID: 154791, updated on 2-Nov-2024Gene type: protein coding
Also known as: C7orf55; HSPC268
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- Go to complete Gene record for FMC1
- Go to Variation Viewer for FMC1 variants
Summary
Involved in mitochondrial proton-transporting ATP synthase complex assembly. Located in mitochondrion. [provided by Alliance of Genome Resources, Nov 2024]
Genomic context
- Location:
- 7q34
- Sequence:
- Chromosome: 7; NC_000007.14 (139340472..139346328)
- Total number of exons:
- 4
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for FMC1 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
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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