ST20
Suppressor of tumorigenicity 20 protein
Also known as: ST20_HUMAN
Protein identityUniProt · HPA
OverviewNCBI Gene
No narrative summary is available for ST20 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
79 residues, UniProt reviewed canonical sequence.
>Q9HBF5|ST20
1 MARSRLTATS VSQVQENGFV KKLEPKSGWM TFLEVTGKIC EMLFCPEAIL LTRKDTPYCE
61 TGLIFLTLTK TIANTYFYFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ST20 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.53
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)
- 1.76
- gnomAD pLI
- 0.37
- gnomAD missense Z
- 0.04
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ST20 as an antibody target. Whether an autoantibody or antibody against ST20 could matter depends on whether native ST20 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ST20 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 ST20 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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