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 SISNFLocalizationUniProt · 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
- Thioesterase
- Alpha/Beta hydrolase fold
- Thioesterase domain
- Thioesterase type II, NRPS/PKS/S-FAS
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.
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