TASL
TLR adapter interacting with SLC15A4 on the lysosome
Also known as: CXorf21, FLJ11577, TASL_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9HAI6
- Gene
- TASL
- Ensembl
- ENSG00000120280
- Chromosome
- X
- Canonical length
- 301 aa
- Protein class
- Disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles,Cytosol
OverviewNCBI Gene
Involved in positive regulation of toll-like receptor 7 signaling pathway; positive regulation of toll-like receptor 8 signaling pathway; and regulation of lysosomal lumen pH. Located in cytosol; endolysosome membrane; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
301 residues, UniProt reviewed canonical sequence.
>Q9HAI6|TASL
1 MLSEGYLSGL EYWNDIHWSC ASYNEQVAGE KEEETNSVAT LSYSSVDETQ VRSLYVSCKS
61 SGKFISSVHS RESQHSRSQR VTVLQTNPNP VFESPNLAAV EICRDASRET YLVPSSCKSI
121 CKNYNDLQIA GGQVMAINSV TTDFPSESSF EYGPLLKSSE IPLPMEDSIS TQPSDFPQKP
181 IQRYSSYWRI TSIKEKSSLQ MQNPISNAVL NEYLEQKVVE LYKQYIMDTV FHDSSPTQIL
241 ASELIMTSVD QISLQVSREK NLETSKARDI VFSRLLQLMS TEITEISTPS LHISQYSNVN
301 PLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TASL 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.6
- Highest tissue expression
- 18 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 18 nTPM
- appendix: 10 nTPM
- lymph node: 9.8 nTPM
- tonsil: 9.6 nTPM
- spleen: 9.2 nTPM
- thymus: 5.4 nTPM
Single-cell type
- monocyte progenitors: 149 nCPM
- pdcs: 71 nCPM
- cdc: 66 nCPM
- plasma cells: 61 nCPM
- neutrophils: 59 nCPM
- monocytes: 48 nCPM
Immune cell
- plasmacytoid DC: 46 nTPM
- non-classical monocyte: 45 nTPM
- neutrophil: 31 nTPM
- myeloid DC: 25 nTPM
- eosinophil: 24 nTPM
- naive B-cell: 24 nTPM
Brain region
- white matter: 4.8 nTPM
- thalamus: 4.1 nTPM
- pons: 3.5 nTPM
- medulla oblongata: 3.4 nTPM
- choroid plexus: 3.1 nTPM
- spinal cord: 2.7 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)
- 0.49
- gnomAD pLI
- 0.84
- DepMap mean gene effect
- 0.17
- 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
- innate immune response
- positive regulation of innate immune response
- positive regulation of toll-like receptor 7 signaling pathway
- positive regulation of toll-like receptor 8 signaling pathway
- regulation of lysosomal lumen pH
- regulation of toll-like receptor signaling pathway
Cellular components
Protein domainsUniProt · Pfam · InterPro
- TASL protein
- TLR adaptor interacting with SLC15A4 on the lysosome
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TASL in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TASL as an antibody target. Whether an autoantibody or antibody against TASL could matter depends on whether native TASL is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TASL 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 TASL as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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