Seroatlas · Human Serome Atlas

ASCL5

Achaete-scute homolog 5

Also known as: ASCL5_HUMAN

Cross-references: UniProt · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q7RTU5
Gene
ASCL5
Canonical length
278 aa
Protein class
Predicted intracellular proteins

OverviewNCBI Gene

No narrative summary is available for ASCL5 in this catalog release; identity and structured annotations are shown without generated factual claims.

Canonical amino-acid sequenceUniProt

278 residues, UniProt reviewed canonical sequence.

>Q7RTU5|ASCL5
     1  MPMGAAERGA GPQSSAAPWA GSEKAAKRGP SKSWYPRAAA SDVTCPTGGD GADPKPGPFG
    61  GGLALGPAPR GTMNNNFCRA LVDRRPLGPP SCMQLGVMPP PRQAPLPPAE PLGNVPFLLY
   121  PGPAEPPYYD AYAGVFPYVP FPGAFGVYEY PFEPAFIQKR NERERQRVKC VNEGYARLRG
   181  HLPGALAEKR LSKVETLRAA IRYIKYLQEL LSSAPDGSTP PASRGLPGTG PCPAPPATPR
   241  PDRPGDGEAR APSSLVPESS ESSCFSPSPF LESEESWH

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against ASCL5 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)
0.66
Highest tissue expression
1.8 nTPM

Expression across tissuesHPA

Tissue

  • pancreas: 1.8 nTPM
  • basal ganglia: 0.9 nTPM
  • hypothalamus: 0.6 nTPM
  • cerebral cortex: 0.5 nTPM
  • skeletal muscle: 0.5 nTPM
  • amygdala: 0.4 nTPM

Single-cell type

  • thymic myoid cells: 6.8 nCPM
  • cone photoreceptor cells: 2.1 nCPM
  • pancreatic acinar cells: 1.7 nCPM
  • enteric stem cells: 1.5 nCPM
  • other brain neurons: 1.3 nCPM
  • oligodendrocyte progenitor cells: 1.2 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

  • hypothalamus: 3.9 nTPM
  • hippocampal formation: 3.7 nTPM
  • basal ganglia: 3.3 nTPM
  • cerebral cortex: 3.3 nTPM
  • amygdala: 3.1 nTPM
  • midbrain: 2.5 nTPM

DiseaseUniProt · ClinVar · IEDB · PubMed

Four sources answering four different questions about ASCL5.

Disease | GeneticClinVar

1 pathogenic / likely-pathogenic of 1 ClinVar records.

Conditions with pathogenic or likely-pathogenic variants.

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.

DepMap mean gene effect
-0.15
DepMap dependency class
selective

OntologyGO

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads ASCL5 as an antibody target. Whether an autoantibody or antibody against ASCL5 could matter depends on whether native ASCL5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

ASCL5 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 ASCL5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/ASCL5. 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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