TMEM100
Transmembrane protein 100
Also known as: FLJ10970, FLJ37856, TM100_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NV29
- Gene
- TMEM100
- Ensembl
- ENSG00000166292
- Chromosome
- 17
- Canonical length
- 134 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Involved in BMP signaling pathway. Located in several cellular components, including endoplasmic reticulum; perikaryon; and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
134 residues, UniProt reviewed canonical sequence.
>Q9NV29|TMEM100
1 MTEEPIKEIL GAPKAHMAAT MEKSPKSEVV ITTVPLVSEI QLMAATGGTE LSCYRCIIPF
61 AVVVFIAGIV VTAVAYSFNS HGSIISIFGL VVLSSGLFLL ASSALCWKVR QRSKKAKRRE
121 SQTALVANQR SLFALocalizationUniProt · AlphaFold · HPA
Whether an antibody against TMEM100 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 2
- Mean surface accessibility (rSASA)
- 0.51
- Highest tissue expression
- 180 nTPM
Expression across tissuesHPA
Tissue
- lung: 180 nTPM
- placenta: 51 nTPM
- adipose tissue: 38 nTPM
- epididymis: 35 nTPM
- stomach: 29 nTPM
- breast: 27 nTPM
Single-cell type
- lymphatic endothelial cells: 61 nCPM
- vascular endothelial cells: 54 nCPM
- epididymal principal cells: 53 nCPM
- peritubular myoid cells: 50 nCPM
- epididymal efferent duct absorptive cells: 47 nCPM
- fibroblasts: 41 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- hypothalamus: 11 nTPM
- midbrain: 8.6 nTPM
- choroid plexus: 6.4 nTPM
- pons: 6.4 nTPM
- thalamus: 6 nTPM
- basal ganglia: 5.2 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)
- 1.25
- gnomAD pLI
- 0.53
- gnomAD missense Z
- 0.79
- DepMap mean gene effect
- 0.09
- 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
- angiogenesis
- arterial endothelial cell differentiation
- BMP signaling pathway
- cellular response to BMP stimulus
- epithelial to mesenchymal transition involved in endocardial cushion formation
- in utero embryonic development
- Notch signaling pathway
- positive regulation of endothelial cell differentiation
- positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
- positive regulation of vasculogenesis
- regulation of calcium-mediated signaling
- regulation of sensory perception of pain
- vasculogenesis
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Transmembrane protein 100
- Transmembrane protein 100
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TMEM100 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 TMEM100 as an antibody target. Whether an autoantibody or antibody against TMEM100 could matter depends on whether native TMEM100 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TMEM100 is annotated at the cell surface, where native TMEM100 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label TMEM100 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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