Seroatlas · Human Serome Atlas

TES

Testin

Also known as: DKFZP586B2022, TES_HUMAN, TESS-2, TESTIN

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q9UGI8
Gene
TES
Ensembl
ENSG00000135269
Chromosome
7
Canonical length
421 aa
Protein class
Predicted intracellular proteins
Subcellular location
Plasma membrane,Cell Junctions,Focal adhesion sites,Cytosol

OverviewNCBI Gene

Cancer-associated chromosomal changes often involve regions containing fragile sites. This gene maps to a common fragile site on chromosome 7q31.2 designated FRA7G. This gene is similar to mouse Testin, a testosterone-responsive gene encoding a Sertoli cell secretory protein containing three LIM domains. LIM domains are double zinc-finger motifs that mediate protein-protein interactions between transcription factors, cytoskeletal proteins and signaling proteins. This protein is a negative regulator of cell growth and may act as a tumor suppressor. This scaffold protein may also play a role in cell adhesion, cell spreading and in the reorganization of the actin cytoskeleton. Multiple protein isoforms are encoded by transcript variants of this gene.[provided by RefSeq, Aug 2023]

Canonical amino-acid sequenceUniProt

421 residues, UniProt reviewed canonical sequence.

>Q9UGI8|TES
     1  MDLENKVKKM GLGHEQGFGA PCLKCKEKCE GFELHFWRKI CRNCKCGQEE HDVLLSNEED
    61  RKVGKLFEDT KYTTLIAKLK SDGIPMYKRN VMILTNPVAA KKNVSINTVT YEWAPPVQNQ
   121  ALARQYMQML PKEKQPVAGS EGAQYRKKQL AKQLPAHDQD PSKCHELSPR EVKEMEQFVK
   181  KYKSEALGVG DVKLPCEMDA QGPKQMNIPG GDRSTPAAVG AMEDKSAEHK RTQYSCYCCK
   241  LSMKEGDPAI YAERAGYDKL WHPACFVCST CHELLVDMIY FWKNEKLYCG RHYCDSEKPR
   301  CAGCDELIFS NEYTQAENQN WHLKHFCCFD CDSILAGEIY VMVNDKPVCK PCYVKNHAVV
   361  CQGCHNAIDP EVQRVTYNNF SWHASTECFL CSCCSKCLIG QKFMPVEGMV FCSVECKKRM
   421  S

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against TES 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
0
Mean surface accessibility (rSASA)
0.34
Highest tissue expression
186 nTPM

Expression across tissuesHPA

Tissue

  • seminal vesicle: 186 nTPM
  • smooth muscle: 138 nTPM
  • colon: 126 nTPM
  • blood vessel: 96 nTPM
  • endometrium: 93 nTPM
  • urinary bladder: 81 nTPM

Single-cell type

  • early spermatids: 486 nCPM
  • alveolar cells type 1: 444 nCPM
  • endometrial luminal cells: 439 nCPM
  • endometrial glandular cells: 387 nCPM
  • endometrial secretory cells: 338 nCPM
  • neutrophils: 323 nCPM

Immune cell

  • basophil: 276 nTPM
  • eosinophil: 222 nTPM
  • NK-cell: 206 nTPM
  • non-classical monocyte: 171 nTPM
  • total PBMC: 163 nTPM
  • gdT-cell: 151 nTPM

Brain region

  • choroid plexus: 18 nTPM
  • medulla oblongata: 11 nTPM
  • thalamus: 6.3 nTPM
  • cerebral cortex: 5 nTPM
  • midbrain: 4.8 nTPM
  • cerebellum: 4.6 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)
1.55
gnomAD pLI
0
gnomAD missense Z
0.39
DepMap mean gene effect
0.01
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% 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

InteractionsUniProt · HPA

Protein binding partners of TES 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 TES as an antibody target. Whether an autoantibody or antibody against TES could matter depends on whether native TES is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

TES is annotated at the cell surface, where native TES 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 TES as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/TES. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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