HES4
Transcription factor HES-4
Also known as: bHLHb42, HES4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9HCC6
- Gene
- HES4
- Ensembl
- ENSG00000188290
- Chromosome
- 1
- Canonical length
- 221 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm,Vesicles,Cytosol
OverviewNCBI Gene
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in cell differentiation; nervous system development; 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
221 residues, UniProt reviewed canonical sequence.
>Q9HCC6|HES4
1 MAADTPGKPS ASPMAGAPAS ASRTPDKPRS AAEHRKSSKP VMEKRRRARI NESLAQLKTL
61 ILDALRKESS RHSKLEKADI LEMTVRHLRS LRRVQVTAAL SADPAVLGKY RAGFHECLAE
121 VNRFLAGCEG VPADVRSRLL GHLAACLRQL GPSRRPASLS PAAPAEAPAP EVYAGRPLLP
181 SLGGPFPLLA PPLLPGLTRA LPAAPRAGPQ GPGGPWRPWL RLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HES4 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)
- 0.58
- Highest tissue expression
- 31 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 31 nTPM
- basal ganglia: 24 nTPM
- heart muscle: 23 nTPM
- hypothalamus: 17 nTPM
- cerebral cortex: 15 nTPM
- amygdala: 14 nTPM
Single-cell type
- vascular smooth muscle cells: 647 nCPM
- urothelial cells: 483 nCPM
- fallopian secretory cells: 434 nCPM
- epididymal efferent duct absorptive cells: 416 nCPM
- pericytes: 356 nCPM
- respiratory secretory cells: 290 nCPM
Immune cell
- eosinophil: 13 nTPM
- non-classical monocyte: 1.3 nTPM
- intermediate monocyte: 1 nTPM
- myeloid DC: 0.3 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
Brain region
- cerebral cortex: 90 nTPM
- thalamus: 64 nTPM
- medulla oblongata: 60 nTPM
- hypothalamus: 51 nTPM
- pons: 50 nTPM
- midbrain: 47 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)
- 1.95
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.47
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- anterior/posterior pattern specification
- cell differentiation
- nervous system development
- 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 HES4 as an antibody target. Whether an autoantibody or antibody against HES4 could matter depends on whether native HES4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HES4 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 HES4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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