TEPSIN
AP-4 complex accessory subunit Tepsin
Also known as: AP4AT_HUMAN, C17orf56, ENTHD2, FLJ31528
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96N21
- Gene
- TEPSIN
- Ensembl
- ENSG00000167302
- Chromosome
- 17
- Canonical length
- 525 aa
- Protein class
- Predicted intracellular proteins, Transporters
- Subcellular location
- Vesicles
OverviewNCBI Gene
Located in coated vesicle membrane and trans-Golgi network membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
525 residues, UniProt reviewed canonical sequence.
>Q96N21|TEPSIN
1 MAAAPPLRDR LSFLHRLPIL LKGTSDDDVP CPGYLFEEIA KISHESPGSS QCLLEYLLSR
61 LHSSSGHGKL KVLKILLYLC SHGSSFFLLI LKRNSAFIQE AAAFAGPPDP LHGNSLYQKV
121 RAAAQDLGST LFSDTVLPLA PSQPLGTPPA TGMGSQARPH STLQGFGYSK EHGRTAVRHQ
181 PGQAGGGWDE LDSGPSSQNS SQNSDLSRVS DSGSHSGSDS HSGASREPGD LAERVEVVAL
241 SDCQQELSLV RTVTRGPRAF LSREEAQHFI KACGLLNCEA VLQLLTCHLR GTSECTQLRA
301 LCAIASLGSS DLLPQEHILL RTRPWLQELS MGSPGPVTNK ATKILRHFEA SCGQLSPARG
361 TSAEPGPTAA LPGPSDLLTD AVPLPGSQVF LQPLSSTPVS SRSPAPSSGM PSSPVPTPPP
421 DASPIPAPGD PSEAEARLAE SRRWRPERIP GGTDSPKRGP SSCAWSRDSL FAGMELVACP
481 RLVGAGAAAG ESCPDAPRAP QTSSQRTAAK EPPGSEPSAF AFLNALocalizationUniProt · AlphaFold · HPA
Whether an antibody against TEPSIN 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
- 0
- Mean surface accessibility (rSASA)
- 0.52
- Highest tissue expression
- 33 nTPM
Expression across tissuesHPA
Tissue
- spleen: 33 nTPM
- small intestine: 22 nTPM
- liver: 20 nTPM
- thyroid gland: 19 nTPM
- kidney: 18 nTPM
- prostate: 18 nTPM
Single-cell type
- tuft cells: 46 nCPM
- microglia: 19 nCPM
- neutrophils: 16 nCPM
- late primary spermatocytes: 15 nCPM
- differentiating spermatogonia: 14 nCPM
- early primary spermatocytes: 13 nCPM
Immune cell
- eosinophil: 4 nTPM
- basophil: 2.4 nTPM
- neutrophil: 2.1 nTPM
- naive B-cell: 1.8 nTPM
- intermediate monocyte: 1.6 nTPM
- plasmacytoid DC: 1.4 nTPM
Brain region
- medulla oblongata: 8.7 nTPM
- choroid plexus: 8.3 nTPM
- thalamus: 8.2 nTPM
- cerebral cortex: 7.8 nTPM
- pons: 7.8 nTPM
- white matter: 7.2 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)
- 1.28
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.18
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
- cytoplasm
- cytosol
- organelle membrane
- trans-Golgi network membrane
- coated vesicle membrane
Protein domainsUniProt · Pfam · InterPro
- ENTH/VHS
- ENTH domain
- ENTH domain
- Tepsin, ENTH/VHS domain
- AP-4 complex accessory subunit Tepsin
- AP-4 complex accessory subunit Tepsin, VHS/ENTH-like domain
- Tepsin VHS/ENTH-like domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TEPSIN 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 TEPSIN as an antibody target. Whether an autoantibody or antibody against TEPSIN could matter depends on whether native TEPSIN is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TEPSIN 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 TEPSIN as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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