TIMM29
Mitochondrial import inner membrane translocase subunit Tim29
Also known as: C19orf52, TIM29, TIM29_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BSF4
- Gene
- TIMM29
- Ensembl
- ENSG00000142444
- Chromosome
- 19
- Canonical length
- 260 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Mitochondria
OverviewNCBI Gene
Enables protein transporter activity. Involved in protein insertion into mitochondrial inner membrane. Located in mitochondrial inner membrane and mitochondrial intermembrane space. Part of TIM22 mitochondrial import inner membrane insertion complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
260 residues, UniProt reviewed canonical sequence.
>Q9BSF4|TIMM29
1 MAAAALRRFW SRRRAEAGDA VVAKPGVWAR LGSWARALLR DYAEACRDAS AEARARPGRA
61 AVYVGLLGGA AACFTLAPSE GAFEEALLEA SGTLLLLAPA TRNRESEAFV QRLLWLRGRG
121 RLRYVNLGLC SLVYEAPFDA QASLYQARCR YLQPRWTDFP GRVLDVGFVG RWWVLGAWMR
181 DCDINDDEFL HLPAHLRVVG PQQLHSETNE RLFDEKYKPV VLTDDQVDQA LWEEQVLQKE
241 KKDRLALSQA HSLVQAEAPRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TIMM29 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)
- 0.44
- Highest tissue expression
- 24 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 24 nTPM
- esophagus: 15 nTPM
- skin: 14 nTPM
- heart muscle: 14 nTPM
- testis: 13 nTPM
- liver: 13 nTPM
Single-cell type
- early primary spermatocytes: 124 nCPM
- esophageal apical cells: 60 nCPM
- differentiating spermatogonia: 49 nCPM
- syncytiotrophoblasts: 46 nCPM
- cytotrophoblasts: 44 nCPM
- migrating cytotrophoblasts: 40 nCPM
Immune cell
- memory B-cell: 18 nTPM
- naive B-cell: 15 nTPM
- T-reg: 13 nTPM
- memory CD8 T-cell: 12 nTPM
- NK-cell: 11 nTPM
- plasmacytoid DC: 11 nTPM
Brain region
- medulla oblongata: 19 nTPM
- cerebral cortex: 18 nTPM
- hippocampal formation: 17 nTPM
- amygdala: 16 nTPM
- midbrain: 16 nTPM
- thalamus: 16 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)
- 1.68
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.62
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% 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
- Mitochondrial import inner membrane translocase subunit Tim29
- Translocase of the Inner Mitochondrial membrane 29
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TIMM29 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 TIMM29 as an antibody target. Whether an autoantibody or antibody against TIMM29 could matter depends on whether native TIMM29 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TIMM29 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 TIMM29 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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