MICOS13
MICOS complex subunit MIC13
Also known as: C19orf70, MIC12, MIC13, MIC13_HUMAN, P117, QIL1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5XKP0
- Gene
- MICOS13
- Ensembl
- ENSG00000174917
- Chromosome
- 19
- Canonical length
- 118 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Mitochondria
OverviewNCBI Gene
Involved in cristae formation. Located in mitochondrial crista junction and nucleoplasm. Part of MICOS complex. Implicated in combined oxidative phosphorylation deficiency 37. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
118 residues, UniProt reviewed canonical sequence.
>Q5XKP0|MICOS13
1 MVARVWSLMR FLIKGSVAGG AVYLVYDQEL LGPSDKSQAA LQKAGEVVPP AMYQFSQYVC
61 QQTGLQIPQL PAPPKIYFPI RDSWNAGIMT VMSALSVAPS KAREYSKEGW EYVKARTKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MICOS13 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.48
- Highest tissue expression
- 343 nTPM
Expression across tissuesHPA
Tissue
- heart muscle: 343 nTPM
- skeletal muscle: 304 nTPM
- midbrain: 207 nTPM
- amygdala: 205 nTPM
- cerebral cortex: 193 nTPM
- basal ganglia: 179 nTPM
Single-cell type
- late spermatids: 6,711 nCPM
- early spermatids: 945 nCPM
- esophageal suprabasal cells: 404 nCPM
- colonocytes: 390 nCPM
- parietal cells: 375 nCPM
- esophageal basal cells: 357 nCPM
Immune cell
- plasmacytoid DC: 303 nTPM
- memory B-cell: 293 nTPM
- total PBMC: 279 nTPM
- intermediate monocyte: 276 nTPM
- myeloid DC: 262 nTPM
- non-classical monocyte: 240 nTPM
Brain region
- hypothalamus: 134 nTPM
- cerebellum: 131 nTPM
- thalamus: 130 nTPM
- medulla oblongata: 122 nTPM
- pons: 120 nTPM
- white matter: 115 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about MICOS13.
Disease | AllUniProt
Conditions MICOS13 is implicated in, by any mechanism.
- Combined oxidative phosphorylation deficiency 37 (COXPD37) MIM:618329
Disease | GeneticClinVar
7 pathogenic / likely-pathogenic of 36 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Combined oxidative phosphorylation deficiency 37
- Inborn genetic diseases
- Intellectual developmental disorder with autism and macrocephaly
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.63
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.19
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
- MICOS complex subunit Mic13
- MICOS complex subunit MIC13, QIL1
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MICOS13 as an antibody target. Whether an autoantibody or antibody against MICOS13 could matter depends on whether native MICOS13 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MICOS13 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label MICOS13 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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