Seroatlas · Human Serome Atlas

TIMM10B

Mitochondrial import inner membrane translocase subunit Tim10 B

Also known as: FXC1, T10B_HUMAN, TIM10B, Tim9b

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q9Y5J6
Gene
TIMM10B
Ensembl
ENSG00000132286
Chromosome
11
Canonical length
103 aa
Protein class
Predicted intracellular proteins

OverviewNCBI Gene

FXC1, or TIMM10B, belongs to a family of evolutionarily conserved proteins that are organized in heterooligomeric complexes in the mitochondrial intermembrane space. These proteins mediate the import and insertion of hydrophobic membrane proteins into the mitochondrial inner membrane.[supplied by OMIM, Apr 2004]

Canonical amino-acid sequenceUniProt

103 residues, UniProt reviewed canonical sequence.

>Q9Y5J6|TIMM10B
     1  MERQQQQQQQ LRNLRDFLLV YNRMTELCFQ RCVPSLHHRA LDAEEEACLH SCAGKLIHSN
    61  HRLMAAYVQL MPALVQRRIA DYEAASAVPG VAAEQPGVSP SGS

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against TIMM10B 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)
0.51
Highest tissue expression
27 nTPM

Expression across tissuesHPA

Tissue

  • parathyroid gland: 27 nTPM
  • thyroid gland: 25 nTPM
  • kidney: 25 nTPM
  • adrenal gland: 24 nTPM
  • pancreas: 23 nTPM
  • blood vessel: 23 nTPM

Single-cell type

  • early primary spermatocytes: 5.2 nCPM
  • early spermatids: 3.5 nCPM
  • late primary spermatocytes: 3.2 nCPM
  • gastric progenitor cells: 2.6 nCPM
  • syncytiotrophoblasts: 2.6 nCPM
  • differentiating spermatogonia: 2.5 nCPM

Immune cell

  • naive CD4 T-cell: 45 nTPM
  • naive CD8 T-cell: 40 nTPM
  • total PBMC: 40 nTPM
  • MAIT T-cell: 39 nTPM
  • naive B-cell: 38 nTPM
  • gdT-cell: 37 nTPM

Brain region

  • pons: 47 nTPM
  • midbrain: 46 nTPM
  • medulla oblongata: 44 nTPM
  • cerebral cortex: 42 nTPM
  • white matter: 41 nTPM
  • hypothalamus: 41 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)
1.92
gnomAD pLI
0
gnomAD missense Z
-0.49
DepMap mean gene effect
-0.03
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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of TIMM10B 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 TIMM10B as an antibody target. Whether an autoantibody or antibody against TIMM10B could matter depends on whether native TIMM10B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

TIMM10B 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 TIMM10B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/TIMM10B. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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