TMPRSS11E
Transmembrane protease serine 11E
Also known as: DESC1, TM11E_HUMAN, TMPRSS11E2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UL52
- Gene
- TMPRSS11E
- Ensembl
- ENSG00000087128
- Chromosome
- 4
- Canonical length
- 423 aa
- Protein class
- Enzymes, Predicted membrane proteins, Predicted secreted proteins
- Subcellular location
- Golgi apparatus
- Secretome location
- Secreted in other tissues
OverviewNCBI Gene
Predicted to enable serine-type peptidase activity. Involved in cognition. Predicted to be located in extracellular region and membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
423 residues, UniProt reviewed canonical sequence.
>Q9UL52|TMPRSS11E
1 MMYRPDVVRA RKRVCWEPWV IGLVIFISLI VLAVCIGLTV HYVRYNQKKT YNYYSTLSFT
61 TDKLYAEFGR EASNNFTEMS QRLESMVKNA FYKSPLREEF VKSQVIKFSQ QKHGVLAHML
121 LICRFHSTED PETVDKIVQL VLHEKLQDAV GPPKVDPHSV KIKKINKTET DSYLNHCCGT
181 RRSKTLGQSL RIVGGTEVEE GEWPWQASLQ WDGSHRCGAT LINATWLVSA AHCFTTYKNP
241 ARWTASFGVT IKPSKMKRGL RRIIVHEKYK HPSHDYDISL AELSSPVPYT NAVHRVCLPD
301 ASYEFQPGDV MFVTGFGALK NDGYSQNHLR QAQVTLIDAT TCNEPQAYND AITPRMLCAG
361 SLEGKTDACQ GDSGGPLVSS DARDIWYLAG IVSWGDECAK PNKPGVYTRV TALRDWITSK
421 TGILocalizationUniProt · AlphaFold · HPA
Whether an antibody against TMPRSS11E 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)
- 0.27
- Highest tissue expression
- 210 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 210 nTPM
- vagina: 156 nTPM
- cervix: 116 nTPM
- salivary gland: 50 nTPM
- tonsil: 23 nTPM
- epididymis: 17 nTPM
Single-cell type
- esophageal apical cells: 676 nCPM
- salivary ionocytes: 331 nCPM
- respiratory ionocytes: 71 nCPM
- prostatic hillock cells: 25 nCPM
- esophageal suprabasal cells: 25 nCPM
- salivary duct cells: 20 nCPM
Immune cell
- memory B-cell: 0.2 nTPM
- naive B-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 nTPM
- cerebral cortex: 0 nTPM
- choroid plexus: 0 nTPM
- hippocampal formation: 0 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)
- 0.91
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.31
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TMPRSS11E as an antibody target. Whether an autoantibody or antibody against TMPRSS11E could matter depends on whether native TMPRSS11E is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TMPRSS11E is annotated at the cell surface, where native TMPRSS11E 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 TMPRSS11E as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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