TMEM106A
Transmembrane protein 106A
Also known as: MGC20235, T106A_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96A25
- Gene
- TMEM106A
- Ensembl
- ENSG00000184988
- Chromosome
- 17
- Canonical length
- 262 aa
- Protein class
- Predicted membrane proteins, Transporters
OverviewNCBI Gene
Predicted to be involved in several processes, including positive regulation of intracellular signal transduction; positive regulation of macromolecule biosynthetic process; and positive regulation of nitric oxide metabolic process. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
262 residues, UniProt reviewed canonical sequence.
>Q96A25|TMEM106A
1 MGKTFSQLGS WREDENKSIL SSKPAIGSKA VNYSSTGSSK SFCSCVPCEG TADASFVTCP
61 TCQGSGKIPQ ELEKQLVALI PYGDQRLKPK HTKLFVFLAV LICLVTSSFI VFFLFPRSVI
121 VQPAGLNSST VAFDEADIYL NITNILNISN GNYYPIMVTQ LTLEVLHLSL VVGQVSNNLL
181 LHIGPLASEQ MFYAVATKIR DENTYKICTW LEIKVHHVLL HIQGTLTCSY LSHSEQLVFQ
241 SYEYVDCRGN ASVPHQLTPH PPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TMEM106A 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
- 1
- Mean surface accessibility (rSASA)
- 0.46
- Highest tissue expression
- 20 nTPM
Expression across tissuesHPA
Tissue
- kidney: 20 nTPM
- appendix: 9.6 nTPM
- placenta: 9.5 nTPM
- spleen: 9.1 nTPM
- smooth muscle: 8.3 nTPM
- lymph node: 6.5 nTPM
Single-cell type
- hofbauer cells: 108 nCPM
- proximal tubule cells: 95 nCPM
- microglia: 69 nCPM
- macrophages: 66 nCPM
- kupffer cells: 62 nCPM
- monocytes: 52 nCPM
Immune cell
- basophil: 27 nTPM
- plasmacytoid DC: 6 nTPM
- eosinophil: 5.7 nTPM
- intermediate monocyte: 5.6 nTPM
- classical monocyte: 5.1 nTPM
- myeloid DC: 4.2 nTPM
Brain region
- thalamus: 19 nTPM
- medulla oblongata: 19 nTPM
- white matter: 14 nTPM
- pons: 14 nTPM
- cerebral cortex: 13 nTPM
- midbrain: 12 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)
- 1.48
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.58
- DepMap mean gene effect
- -0.14
- 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
- glycoprotein biosynthetic process
- innate immune response
- macrophage activation
- positive regulation of canonical NF-kappaB signal transduction
- positive regulation of interleukin-1 beta production
- positive regulation of interleukin-6 production
- positive regulation of MAPK cascade
- positive regulation of MHC class II biosynthetic process
- positive regulation of nitric oxide metabolic process
- positive regulation of tumor necrosis factor production
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TMEM106A 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 TMEM106A as an antibody target. Whether an autoantibody or antibody against TMEM106A could matter depends on whether native TMEM106A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TMEM106A is annotated at the cell surface, where native TMEM106A 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 TMEM106A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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