Seroatlas · Human Serome Atlas

TXNL1

Thioredoxin-like protein 1

Also known as: TRP32, Txl, TXNL, TXNL1_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
O43396
Gene
TXNL1
Ensembl
ENSG00000091164
Chromosome
18
Canonical length
289 aa
Protein class
Plasma proteins, Predicted intracellular proteins
Subcellular location
Cytosol

OverviewNCBI Gene

Enables disulfide oxidoreductase activity. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

289 residues, UniProt reviewed canonical sequence.

>O43396|TXNL1
     1  MVGVKPVGSD PDFQPELSGA GSRLAVVKFT MRGCGPCLRI APAFSSMSNK YPQAVFLEVD
    61  VHQCQGTAAT NNISATPTFL FFRNKVRIDQ YQGADAVGLE EKIKQHLEND PGSNEDTDIP
   121  KGYMDLMPFI NKAGCECLNE SDEHGFDNCL RKDTTFLESD CDEQLLITVA FNQPVKLYSM
   181  KFQGPDNGQG PKYVKIFINL PRSMDFEEAE RSEPTQALEL TEDDIKEDGI VPLRYVKFQN
   241  VNSVTIFVQS NQGEEETTRI SYFTFIGTPV QATNMNDFKR VVGKKGESH

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against TXNL1 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)
0.27
Highest tissue expression
185 nTPM

Expression across tissuesHPA

Tissue

  • thyroid gland: 185 nTPM
  • skeletal muscle: 140 nTPM
  • tongue: 137 nTPM
  • bone marrow: 78 nTPM
  • liver: 75 nTPM
  • heart muscle: 75 nTPM

Single-cell type

  • esophageal apical cells: 612 nCPM
  • syncytiotrophoblasts: 477 nCPM
  • late spermatids: 428 nCPM
  • esophageal suprabasal cells: 329 nCPM
  • late primary spermatocytes: 296 nCPM
  • cytotrophoblasts: 293 nCPM

Immune cell

  • basophil: 99 nTPM
  • classical monocyte: 63 nTPM
  • total PBMC: 62 nTPM
  • intermediate monocyte: 56 nTPM
  • non-classical monocyte: 55 nTPM
  • myeloid DC: 55 nTPM

Brain region

  • white matter: 60 nTPM
  • cerebral cortex: 58 nTPM
  • hypothalamus: 57 nTPM
  • pons: 53 nTPM
  • cerebellum: 52 nTPM
  • hippocampal formation: 52 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)
0.4
gnomAD pLI
0.89
gnomAD missense Z
1.52
DepMap mean gene effect
-0.09
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of TXNL1 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 TXNL1 as an antibody target. Whether an autoantibody or antibody against TXNL1 could matter depends on whether native TXNL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

TXNL1 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 TXNL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/TXNL1. 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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