Seroatlas · Human Serome Atlas

STATH

Statherin

Also known as: STAT_HUMAN, STR

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

Protein identityUniProt · HPA

UniProt accession
P02808
Gene
STATH
Ensembl
ENSG00000126549
Chromosome
4
Canonical length
62 aa
Protein class
Plasma proteins, Predicted secreted proteins, Transporters
Secretome location
Secreted to digestive system

OverviewNCBI Gene

Predicted to enable extracellular matrix constituent, lubricant activity and hydroxyapatite binding activity. Predicted to be a structural constituent of tooth enamel. Predicted to be involved in negative regulation of bone mineralization; ossification; and saliva secretion. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

62 residues, UniProt reviewed canonical sequence.

>P02808|STATH
     1  MKFLVFAFIL ALMVSMIGAD SSEEKFLRRI GRFGYGYGPY QPVPEQPLYP QPYQPQYQQY
    61  TF

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against STATH 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
Secreted
Secreted
Yes
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.65
Highest tissue expression
8,578 nTPM

Expression across tissuesHPA

Tissue

  • salivary gland: 8,578 nTPM
  • pancreas: 9.3 nTPM
  • pituitary gland: 6.5 nTPM
  • tongue: 3.1 nTPM
  • esophagus: 2.8 nTPM
  • heart muscle: 1.7 nTPM

Single-cell type

  • salivary acinar cells: 59,340 nCPM
  • salivary myoepithelial cells: 15,709 nCPM
  • neutrophils: 2,049 nCPM
  • submucosal glandular cells: 1,292 nCPM
  • salivary basal cells: 610 nCPM
  • lacrimal acinar cells: 310 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

  • 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)
1.81
gnomAD pLI
0
gnomAD missense Z
-0.31
DepMap mean gene effect
0.13
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 1% 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 STATH as an antibody target. Whether an autoantibody or antibody against STATH could matter depends on whether native STATH is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

STATH is annotated as secreted, so native STATH circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.

Annotation status

The present source text does not explicitly label STATH as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/STATH. 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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