TOMM20
Mitochondrial import receptor subunit TOM20 homolog
Also known as: KIAA0016, MAS20, MOM19, TOM20, TOM20_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q15388
- Gene
- TOMM20
- Ensembl
- ENSG00000173726
- Chromosome
- 1
- Canonical length
- 145 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Mitochondria
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables mitochondrion targeting sequence binding activity; protein-transporting ATPase activity; and unfolded protein binding activity. Involved in protein targeting to mitochondrion. Located in mitochondria-associated endoplasmic reticulum membrane contact site and mitochondrial outer membrane. Is active in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
145 residues, UniProt reviewed canonical sequence.
>Q15388|TOMM20
1 MVGRNSAIAA GVCGALFIGY CIYFDRKRRS DPNFKNRLRE RRKKQKLAKE RAGLSKLPDL
61 KDAEAVQKFF LEEIQLGEEL LAQGEYEKGV DHLTNAIAVC GQPQQLLQVL QQTLPPPVFQ
121 MLLTKLPTIS QRIVSAQSLA EDDVELocalizationUniProt · AlphaFold · HPA
Whether an antibody against TOMM20 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)
- 0.43
- Highest tissue expression
- 134 nTPM
Expression across tissuesHPA
Tissue
- thyroid gland: 134 nTPM
- cerebral cortex: 134 nTPM
- breast: 123 nTPM
- spinal cord: 121 nTPM
- salivary gland: 118 nTPM
- basal ganglia: 113 nTPM
Single-cell type
- gastric progenitor cells: 1,086 nCPM
- extravillous trophoblasts: 542 nCPM
- late spermatids: 451 nCPM
- late primary spermatocytes: 423 nCPM
- lacrimal acinar cells: 373 nCPM
- fallopian secretory cells: 355 nCPM
Immune cell
- basophil: 38 nTPM
- plasmacytoid DC: 31 nTPM
- naive CD4 T-cell: 30 nTPM
- memory CD4 T-cell: 25 nTPM
- memory CD8 T-cell: 24 nTPM
- naive CD8 T-cell: 24 nTPM
Brain region
- cerebral cortex: 146 nTPM
- basal ganglia: 140 nTPM
- hypothalamus: 131 nTPM
- spinal cord: 130 nTPM
- white matter: 127 nTPM
- pons: 125 nTPM
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)
- 0.94
- gnomAD pLI
- 0.03
- gnomAD missense Z
- 1.58
- DepMap mean gene effect
- -0.66
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 10% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- intracellular protein transport
- protein import into mitochondrial matrix
- protein insertion into mitochondrial outer membrane
- protein targeting to mitochondrion
- tRNA import into mitochondrion
Molecular functions
- mitochondrion targeting sequence binding
- unfolded protein binding
- protein-transporting ATPase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TOMM20 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TOMM20 as an antibody target. Whether an autoantibody or antibody against TOMM20 could matter depends on whether native TOMM20 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TOMM20 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 TOMM20 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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