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GeneE
3 sources retrieved Β· Most recent: April 2026 Β· Index updated 14 days ago
β“˜GeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
TMEM186
transmembrane protein 186
Chromosome 16 Β· 16p13.2
NCBI Gene: 25880Ensembl: ENSG00000184857.9HGNC: HGNC:24530UniProt: Q96B77
20PubMed Papers
12Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
βœ“ Experimental GO Evidenceβœ“ Swiss-Prot Reviewed
protein bindingmitochondrial respiratory chain complex I assemblymitochondrionmitochondrial complex I intermediate assembly complexPMM2-congenital disorder of glycosylationcongenital disorder of glycosylationosteonecrosisprimary thrombocytopenia
✦AI Summary

TMEM186 is a transmembrane protein localized to the mitochondrial inner membrane that functions as a component of the mitochondrial complex I intermediate assembly (MCIA) complex. As part of the MCIA complex alongside NDUFAF1, ECSIT, ACAD9, and TMEM126B, TMEM186 is required for efficient assembly of mitochondrial respiratory chain complex I 1. The protein enriches with newly translated ND3 subunit during complex I biogenesis and is essential for the assembly and integration of the ND2-module, a distinct intermediate in the stepwise construction of complex I 1. Loss of TMEM186 results in defects of the MCIA complex and reduced overall complex I assembly 1. TMEM186 belongs to the TMEM70/TMEM186/TMEM223 protein family, which is evolutionarily conserved only in species possessing oxidative phosphorylation (OXPHOS) complexes, suggesting a specialized role in mitochondrial bioenergetics 2. By supporting complex I assembly, TMEM186 contributes to proper mitochondrial function and oxidative energy production, though specific disease associations remain to be established.

Sources cited
1
TMEM186 is a bona fide MCIA complex component required for complex I assembly and ND3 enrichment
PMID: 32320651
2
TMEM186 belongs to evolutionarily conserved TMEM70/TMEM186/TMEM223 family present only in OXPHOS-containing species
PMID: 32275929
⚠Limited data available β€” This gene has 2 indexed publications. Summary and analysis may be incomplete.
Disease Associationsβ“˜12
congenital disorder of glycosylationOpen Targets
0.38Weak
PMM2-congenital disorder of glycosylationOpen Targets
0.38Weak
osteonecrosisOpen Targets
0.06Suggestive
primary thrombocytopeniaOpen Targets
0.05Suggestive
systemic juvenile idiopathic arthritisOpen Targets
0.01Suggestive
cancerOpen Targets
0.00Suggestive
Alzheimer diseaseOpen Targets
0.00Suggestive
acute myeloid leukemiaOpen Targets
0.00Suggestive
Hereditary breast cancerOpen Targets
0.00Suggestive
hereditary breast carcinomaOpen Targets
0.00Suggestive
nonpapillary renal cell carcinomaOpen Targets
0.00Suggestive
thyroid cancer, nonmedullary, 1Open Targets
0.00Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar β†—
Related Genes
NDUFAF8Shared pathway100%DMAC1Shared pathway100%NDUFAF5Shared pathway100%LYRM2Shared pathway100%FOXRED1Shared pathway100%NDUFAF6Protein interaction90%
Tissue Expression6 tissues
Liver
100%
Heart
80%
Brain
58%
Lung
43%
Ovary
42%
Bone Marrow
13%
Gene Interaction Network
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TMEM186NDUFAF8DMAC1NDUFAF5LYRM2FOXRED1NDUFAF6
PROTEIN STRUCTURE
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AlphaFoldAI-predicted Β· UniProt Q96B77
View on AlphaFold β†—
Constraintβ“˜
LOEUFβ“˜
1.81LoF Tolerant
pLIβ“˜
0.02Tolerant
Observed/Expected LoF0.96 [0.46–1.81]
RankingsWhere TMEM186 stands among ~20K protein-coding genes
  • #14,297of 20,598
    Most Researched20
  • #16,627of 17,882
    Most Constrained (LOEUF)1.81
Genes detectedTMEM186
Sources retrieved3 papers
Response timeβ€”
πŸ“„ Sources
3
1
TMEM70 functions in the assembly of complexes I and V.
PMID: 32275929
Biochim Biophys Acta Bioenerg Β· 2020
1.00
2
Dissecting the Roles of Mitochondrial Complex I Intermediate Assembly Complex Factors in the Biogenesis of Complex I.
PMID: 32320651
Cell Rep Β· 2020
0.67
3
EARS2 significantly coexpresses with PALB2 in breast and pancreatic cancer.
PMID: 35779338
Cancer Treat Res Commun Β· 2022
0.33