TOMM34
Mitochondrial import receptor subunit TOM34
Also known as: HTOM34P, TOM34, TOM34_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q15785
- Gene
- TOMM34
- Ensembl
- ENSG00000025772
- Chromosome
- 20
- Canonical length
- 309 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles,Mitochondria,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is involved in the import of precursor proteins into mitochondria. The encoded protein has a chaperone-like activity, binding the mature portion of unfolded proteins and aiding their import into mitochondria. This protein, which is found in the cytoplasm and sometimes associated with the outer mitochondrial membrane, has a weak ATPase activity and contains 6 TPR repeats. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
309 residues, UniProt reviewed canonical sequence.
>Q15785|TOMM34
1 MAPKFPDSVE ELRAAGNESF RNGQYAEASA LYGRALRVLQ AQGSSDPEEE SVLYSNRAAC
61 HLKDGNCRDC IKDCTSALAL VPFSIKPLLR RASAYEALEK YPMAYVDYKT VLQIDDNVTS
121 AVEGINRMTR ALMDSLGPEW RLKLPSIPLV PVSAQKRWNS LPSENHKEMA KSKSKETTAT
181 KNRVPSAGDV EKARVLKEEG NELVKKGNHK KAIEKYSESL LCSNLESATY SNRALCYLVL
241 KQYTEAVKDC TEALKLDGKN VKAFYRRAQA HKALKDYKSS FADISNLLQI EPRNGPAQKL
301 RQEVKQNLHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TOMM34 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
- 0
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 119 nTPM
Expression across tissuesHPA
Tissue
- testis: 119 nTPM
- basal ganglia: 88 nTPM
- hippocampal formation: 66 nTPM
- adrenal gland: 46 nTPM
- epididymis: 46 nTPM
- fallopian tube: 46 nTPM
Single-cell type
- oocytes: 207 nCPM
- cytotrophoblasts: 163 nCPM
- migrating cytotrophoblasts: 95 nCPM
- undifferentiated spermatogonia: 82 nCPM
- urothelial cells: 78 nCPM
- late primary spermatocytes: 71 nCPM
Immune cell
- myeloid DC: 40 nTPM
- naive B-cell: 29 nTPM
- memory B-cell: 26 nTPM
- plasmacytoid DC: 21 nTPM
- T-reg: 19 nTPM
- non-classical monocyte: 19 nTPM
Brain region
- hippocampal formation: 82 nTPM
- cerebral cortex: 75 nTPM
- basal ganglia: 52 nTPM
- white matter: 41 nTPM
- hypothalamus: 38 nTPM
- amygdala: 33 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TOMM34.
Disease | ImmuneIEDB
Conditions an epitope on TOMM34 was assayed in.
- colorectal adenocarcinoma T cell
- colorectal cancer T cell
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)
- 0.71
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 1.22
- DepMap mean gene effect
- 0.07
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 11% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TOMM34 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 TOMM34 as an antibody target. Whether an autoantibody or antibody against TOMM34 could matter depends on whether native TOMM34 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TOMM34 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 TOMM34 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...