Seroatlas · Human Serome Atlas

ASCL3

Achaete-scute homolog 3

Also known as: ASCL3_HUMAN, bHLHa42, HASH3, Sgn1

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

Protein identityUniProt · HPA

UniProt accession
Q9NQ33
Gene
ASCL3
Ensembl
ENSG00000176009
Chromosome
11
Canonical length
181 aa
Protein class
Predicted intracellular proteins, Transcription factors

OverviewNCBI Gene

Basic helix-loop-helix transcription factors, such as ASCL3, are essential for the determination of cell fate and the development and differentiation of numerous tissues (Jonsson et al., 2004 [PubMed 15475265]).[supplied by OMIM, Mar 2008]

Canonical amino-acid sequenceUniProt

181 residues, UniProt reviewed canonical sequence.

>Q9NQ33|ASCL3
     1  MMDNRGNSSL PDKLPIFPDS ARLPLTRSFY LEPMVTFHVH PEAPVSSPYS EELPRLPFPS
    61  DSLILGNYSE PCPFSFPMPY PNYRGCEYSY GPAFTRKRNE RERQRVKCVN EGYAQLRHHL
   121  PEEYLEKRLS KVETLRAAIK YINYLQSLLY PDKAETKNNP GKVSSMIATT SHHADPMFRI
   181  V

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against ASCL3 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)
0.63
Highest tissue expression
9.5 nTPM

Expression across tissuesHPA

Tissue

  • salivary gland: 9.5 nTPM
  • thymus: 0.5 nTPM
  • kidney: 0.2 nTPM
  • retina: 0.2 nTPM
  • cervix: 0.1 nTPM
  • duodenum: 0.1 nTPM

Single-cell type

  • salivary ionocytes: 1,561 nCPM
  • respiratory ionocytes: 818 nCPM
  • salivary basal cells: 35 nCPM
  • mesothelial cells: 7.2 nCPM
  • conjunctival goblet cells: 6.8 nCPM
  • epicardial cells: 6.8 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

  • cerebellum: 1.3 nTPM
  • medulla oblongata: 1.1 nTPM
  • white matter: 1 nTPM
  • amygdala: 0.9 nTPM
  • cerebral cortex: 0.9 nTPM
  • pons: 0.9 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)
1.65
gnomAD pLI
0.01
gnomAD missense Z
0.12
DepMap mean gene effect
0.06
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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 ASCL3 as an antibody target. Whether an autoantibody or antibody against ASCL3 could matter depends on whether native ASCL3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

ASCL3 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 ASCL3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/ASCL3. 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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