Seroatlas · Human Serome Atlas

RLIG1

RNA ligase 1

Also known as: C12orf29, DKFZp434N2030, RLIG1_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
Q8N999
Gene
RLIG1
Ensembl
ENSG00000133641
Chromosome
12
Canonical length
325 aa
Protein class
Predicted intracellular proteins
Subcellular location
Vesicles

OverviewNCBI Gene

Enables RNA ligase (ATP) activity. Involved in response to reactive oxygen species. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

325 residues, UniProt reviewed canonical sequence.

>Q8N999|RLIG1
     1  MKRLGSVQRK MPCVFVTEVK EEPSSKREHQ PFKVLATETV SHKALDADIY SAIPTEKVDG
    61  TCCYVTTYKD QPYLWARLDR KPNKQAEKRF KNFLHSKENP KEFFWNVEED FKPAPECWIP
   121  AKETEQINGN PVPDENGHIP GWVPVEKNNK QYCWHSSVVN YEFEIALVLK HHPDDSGLLE
   181  ISAVPLSDLL EQTLELIGTN INGNPYGLGS KKHPLHLLIP HGAFQIRNLP SLKHNDLVSW
   241  FEDCKEGKIE GIVWHCSDGC LIKVHRHHLG LCWPIPDTYM NSRPVIINMN LNKCDSAFDI
   301  KCLFNHFLKI DNQKFVRLKD IIFDV

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against RLIG1 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
Unknown
Secreted
No
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.27
Highest tissue expression
15 nTPM

Expression across tissuesHPA

Tissue

  • esophagus: 15 nTPM
  • skin: 15 nTPM
  • epididymis: 12 nTPM
  • liver: 12 nTPM
  • breast: 10 nTPM
  • cerebral cortex: 9.4 nTPM

Single-cell type

  • esophageal apical cells: 460 nCPM
  • oocytes: 157 nCPM
  • esophageal suprabasal cells: 120 nCPM
  • suprabasal keratinocytes: 79 nCPM
  • late primary spermatocytes: 54 nCPM
  • early spermatids: 53 nCPM

Immune cell

  • MAIT T-cell: 4.9 nTPM
  • naive CD4 T-cell: 4.6 nTPM
  • basophil: 4.5 nTPM
  • memory CD4 T-cell: 3.9 nTPM
  • naive CD8 T-cell: 3.9 nTPM
  • NK-cell: 3.4 nTPM

Brain region

  • cerebral cortex: 9.6 nTPM
  • white matter: 9.6 nTPM
  • basal ganglia: 8 nTPM
  • midbrain: 8 nTPM
  • hypothalamus: 7.9 nTPM
  • spinal cord: 7.9 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)
1.36
gnomAD pLI
0
DepMap mean gene effect
-0.09
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Molecular functions

Protein domainsUniProt · Pfam · InterPro

  • RNA ligase 1
  • RNA ligase 1

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads RLIG1 as an antibody target. Whether an autoantibody or antibody against RLIG1 could matter depends on whether native RLIG1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

RLIG1 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 RLIG1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/RLIG1. 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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