Seroatlas · Human Serome Atlas

OLAH

S-acyl fatty acid synthase thioesterase, medium chain

Also known as: FLJ11106, SAST, SAST_HUMAN, THEDC1

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

Protein identityUniProt · HPA

UniProt accession
Q9NV23
Gene
OLAH
Ensembl
ENSG00000152463
Chromosome
10
Canonical length
265 aa
Protein class
Enzymes, Metabolic proteins, Predicted intracellular proteins

OverviewNCBI Gene

Enables fatty acyl-[ACP] hydrolase activity. Involved in medium-chain fatty acid biosynthetic process. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

265 residues, UniProt reviewed canonical sequence.

>Q9NV23|OLAH
     1  MERGDQPKRT RNENIFNCLY KNPEATFKLI CFPWMGGGST HFAKWGQDTH DLLEVHSLRL
    61  PGRESRVEEP LENDISQLVD EVVCALQPVI QDKPFAFFGH SMGSYIAFRT ALGLKENNQP
   121  EPLHLFLSSA TPVHSKAWHR IPKDDELSEE QISHYLMEFG GTPKHFAEAK EFVKQCSPII
   181  RADLNIVRSC TSNVPSKAVL SCDLTCFVGS EDIAKDMEAW KDVTSGNAKI YQLPGGHFYL
   241  LDPANEKLIK NYIIKCLEVS SISNF

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against OLAH 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)
0.26
Highest tissue expression
25 nTPM

Expression across tissuesHPA

Tissue

  • testis: 25 nTPM
  • spleen: 9 nTPM
  • breast: 5.1 nTPM
  • esophagus: 3 nTPM
  • placenta: 3 nTPM
  • salivary gland: 2.5 nTPM

Single-cell type

  • breast lactating cells: 1,785 nCPM
  • early spermatids: 694 nCPM
  • neutrophils: 635 nCPM
  • late primary spermatocytes: 278 nCPM
  • late spermatids: 49 nCPM
  • medullary thymic epithelial cells: 36 nCPM

Immune cell

  • neutrophil: 2.6 nTPM
  • basophil: 0.8 nTPM
  • plasmacytoid DC: 0.5 nTPM
  • NK-cell: 0.4 nTPM
  • memory CD4 T-cell: 0.2 nTPM
  • naive B-cell: 0.2 nTPM

Brain region

  • cerebral cortex: 9.7 nTPM
  • white matter: 9.4 nTPM
  • amygdala: 9 nTPM
  • hippocampal formation: 8.9 nTPM
  • basal ganglia: 8.4 nTPM
  • hypothalamus: 8.3 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)
1.62
gnomAD pLI
0
gnomAD missense Z
-0.97
DepMap mean gene effect
0.1
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 OLAH as an antibody target. Whether an autoantibody or antibody against OLAH could matter depends on whether native OLAH is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

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

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