TMEM109
Voltage-gated monoatomic cation channel TMEM109
Also known as: MGC5508, TM109_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BVC6
- Gene
- TMEM109
- Ensembl
- ENSG00000110108
- Chromosome
- 11
- Canonical length
- 243 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Nuclear membrane,Endoplasmic reticulum,Vesicles,Actin filaments
- Quaternary structure
- Homooligomer
OverviewNCBI Gene
Predicted to enable voltage-gated monoatomic cation channel activity. Acts upstream of or within cellular response to gamma radiation and negative regulation of programmed cell death. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
243 residues, UniProt reviewed canonical sequence.
>Q9BVC6|TMEM109
1 MAASSISSPW GKHVFKAILM VLVALILLHS ALAQSRRDFA PPGQQKREAP VDVLTQIGRS
61 VRGTLDAWIG PETMHLVSES SSQVLWAISS AISVAFFALS GIAAQLLNAL GLAGDYLAQG
121 LKLSPGQVQT FLLWGAGALV VYWLLSLLLG LVLALLGRIL WGLKLVIFLA GFVALMRSVP
181 DPSTRALLLL ALLILYALLS RLTGSRASGA QLEAKVRGLE RQVEELRWRQ RRAAKGARSV
241 EEELocalizationUniProt · AlphaFold · HPA
Whether an antibody against TMEM109 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
- 3
- Mean surface accessibility (rSASA)
- 0.5
- Highest tissue expression
- 119 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 119 nTPM
- endometrium: 96 nTPM
- esophagus: 95 nTPM
- skeletal muscle: 93 nTPM
- adipose tissue: 83 nTPM
- heart muscle: 82 nTPM
Single-cell type
- esophageal apical cells: 182 nCPM
- cytotrophoblasts: 146 nCPM
- extravillous trophoblasts: 141 nCPM
- esophageal basal cells: 133 nCPM
- migrating cytotrophoblasts: 126 nCPM
- pdcs: 116 nCPM
Immune cell
- plasmacytoid DC: 471 nTPM
- myeloid DC: 228 nTPM
- MAIT T-cell: 194 nTPM
- gdT-cell: 189 nTPM
- memory CD8 T-cell: 161 nTPM
- naive B-cell: 141 nTPM
Brain region
- choroid plexus: 74 nTPM
- medulla oblongata: 42 nTPM
- spinal cord: 40 nTPM
- thalamus: 40 nTPM
- pons: 39 nTPM
- midbrain: 36 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)
- 1.19
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.49
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- none
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
- cellular response to gamma radiation
- intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator
- negative regulation of programmed cell death
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Negative regulator of p53/TP53
- Transmembrane protein 109
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TMEM109 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 TMEM109 as an antibody target. Whether an autoantibody or antibody against TMEM109 could matter depends on whether native TMEM109 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TMEM109 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 TMEM109 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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