HES3
Transcription factor HES-3
Also known as: bHLHb43, HES3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5TGS1
- Gene
- HES3
- Ensembl
- ENSG00000173673
- Chromosome
- 1
- Canonical length
- 186 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of neurogenesis. Predicted to act upstream of or within several processes, including nervous system development; regulation of timing of neuron differentiation; and regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
186 residues, UniProt reviewed canonical sequence.
>Q5TGS1|HES3
1 MEKKRRARIN VSLEQLKSLL EKHYSHQIRK RKLEKADILE LSVKYMRSLQ NSLQGLWPVP
61 RGAEQPSGFR SCLPGVSQLL RRGDEVGSGL RCPLVPESAA GSTMDSAGLG QEAPALFRPC
121 TPAVWAPAPA AGGPRSPPPL LLLPESLPGS SASVPPPQPA SSRCAESPGL GLRVWRPWGS
181 PGDDLNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HES3 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.64
- Highest tissue expression
- 0.7 nTPM
Expression across tissuesHPA
Tissue
- thymus: 0.7 nTPM
- testis: 0.1 nTPM
- adipose tissue: 0 nTPM
- adrenal gland: 0 nTPM
- amygdala: 0 nTPM
- appendix: 0 nTPM
Single-cell type
- retinal amacrine cells: 0.7 nCPM
- early spermatids: 0.1 nCPM
- endometrial stromal cells: 0.1 nCPM
- undifferentiated spermatogonia: 0.1 nCPM
- adipocytes: 0 nCPM
- adrenal cortex cells: 0 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
- cerebral cortex: 1 nTPM
- amygdala: 0.7 nTPM
- thalamus: 0.7 nTPM
- hypothalamus: 0.6 nTPM
- midbrain: 0.6 nTPM
- basal ganglia: 0.5 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)
- 1.25
- gnomAD pLI
- 0.28
- gnomAD missense Z
- 0.58
- DepMap mean gene effect
- -0.15
- DepMap dependency class
- selective
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
- anterior/posterior pattern specification
- regulation of neurogenesis
- regulation of transcription by RNA polymerase II
Molecular functions
- DNA-binding transcription factor activity, RNA polymerase II-specific
- protein dimerization activity
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads HES3 as an antibody target. Whether an autoantibody or antibody against HES3 could matter depends on whether native HES3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HES3 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 HES3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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