THNSL1
Threonine synthase-like 1
Also known as: FLJ22002, THNS1_HUMAN, TSH1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IYQ7
- Gene
- THNSL1
- Ensembl
- ENSG00000185875
- Chromosome
- 10
- Canonical length
- 743 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nuclear bodies,Mitochondria,Cytosol
OverviewNCBI Gene
Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
743 residues, UniProt reviewed canonical sequence.
>Q8IYQ7|THNSL1
1 MLHFNRCHHL KKITQKCFSS IHVKTDKHAQ RFLSRTFALA ELRKSWYSTH SLVGDKNIIL
61 MGPPGAGKTT VGRIIGQKLG CCVIDVDDDI LEKTWNMSVS EKLQDVGNEQ FLEEEGKAVL
121 NFSASGSVIS LTGSNPMHDA SMWHLKKNGI IVYLDVPLLD LICRLKLMKT DRIVGQNSGT
181 SMKDLLKFRR QYYKKWYDAR VFCESGASPE EVADKVLNAI KRYQDVDSET FISTRHVWPE
241 DCEQKVSAKF FSEAVIEGLA SDGGLFVPAK EFPKLSCGEW KSLVGATYVE RAQILLERCI
301 HPADIPAARL GEMIETAYGE NFACSKIAPV RHLSGNQFIL ELFHGPTGSF KDLSLQLMPH
361 IFAHCIPPSC NYMILVATSG DTGSAVLNGF SRLNKNDKQR IAVVAFFPEN GVSDFQKAQI
421 IGSQRENGWA VGVESDFDFC QTAIKRIFND SDFTGFLTVE YGTILSSANS INWGRLLPQV
481 VYHASAYLDL VSQGFISFGS PVDVCIPTGN FGNILAAVYA KMMGIPIRKF ICASNQNHVL
541 TDFIKTGHYD LRERKLAQTF SPSIDILKSS NLERHLHLMA NKDGQLMTEL FNRLESQHHF
601 QIEKALVEKL QQDFVADWCS EGECLAAINS TYNTSGYILD PHTAVAKVVA DRVQDKTCPV
661 IISSTAHYSK FAPAIMQALK IKEINETSSS QLYLLGSYNA LPPLHEALLE RTKQQEKMEY
721 QVCAADMNVL KSHVEQLVQN QFILocalizationUniProt · AlphaFold · HPA
Whether an antibody against THNSL1 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)
- 0.24
- Highest tissue expression
- 20 nTPM
Expression across tissuesHPA
Tissue
- liver: 20 nTPM
- kidney: 9.1 nTPM
- thyroid gland: 7.8 nTPM
- ovary: 6.8 nTPM
- adrenal gland: 5.7 nTPM
- testis: 5.5 nTPM
Single-cell type
- other brain neurons: 9.7 nCPM
- brain inhibitory neurons: 9 nCPM
- oligodendrocytes: 8.2 nCPM
- brain excitatory neurons: 7.7 nCPM
- microglia: 7.6 nCPM
- ependymal cells: 6.5 nCPM
Immune cell
- NK-cell: 11 nTPM
- naive CD4 T-cell: 9.5 nTPM
- naive CD8 T-cell: 6.3 nTPM
- MAIT T-cell: 5.1 nTPM
- memory B-cell: 5 nTPM
- memory CD4 T-cell: 4.1 nTPM
Brain region
- hypothalamus: 9.1 nTPM
- cerebral cortex: 8.9 nTPM
- white matter: 8.9 nTPM
- basal ganglia: 8.8 nTPM
- pons: 8.8 nTPM
- spinal cord: 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)
- 1.38
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.47
- DepMap mean gene effect
- 0.13
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Threonine synthase-like
- P-loop containing nucleoside triphosphate hydrolase
- Threonine synthase, N-terminal
- Shikimate kinase/gluconokinase
- Tryptophan synthase beta chain-like, PALP domain superfamily
- Threonine synthase, N-terminal domain superfamily
- Shikimate kinase
- Threonine synthase N terminus
- Shikimate kinase/Threonine synthase-like 1
- Threonine synthase, C-terminal
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads THNSL1 as an antibody target. Whether an autoantibody or antibody against THNSL1 could matter depends on whether native THNSL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
THNSL1 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 THNSL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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