Seroatlas · Human Serome Atlas

SELENOH

Selenoprotein H

Also known as: C11orf31, SELH, SELH_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
Q8IZQ5
Gene
SELENOH
Ensembl
ENSG00000211450
Chromosome
11
Canonical length
122 aa
Protein class
Predicted intracellular proteins
Subcellular location
Nucleoplasm,Nucleoli

OverviewNCBI Gene

This gene encodes a nucleolar protein, which belongs to the SelWTH family. It functions as an oxidoreductase, and has been shown to protect neurons against UVB-induced damage by inhibiting apoptotic cell death pathways, promote mitochondrial biogenesis and mitochondrial function, and suppress cellular senescence through genome maintenance and redox regulation. This protein is a selenoprotein, containing the rare amino acid selenocysteine (Sec) at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2016]

Canonical amino-acid sequenceUniProt

122 residues, UniProt reviewed canonical sequence.

>Q8IZQ5|SELENOH
     1  MAPRGRKRKA EAAVVAVAEK REKLANGGEG MEEATVVIEH CTSURVYGRN AAALSQALRL
    61  EAPELPVKVN PTKPRRGSFE VTLLRPDGSS AELWTGIKKG PPRKLKFPEP QEVVEELKKY
   121  LS

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against SELENOH 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
Highest tissue expression
124 nTPM

Expression across tissuesHPA

Tissue

  • liver: 124 nTPM
  • adrenal gland: 116 nTPM
  • cerebral cortex: 105 nTPM
  • kidney: 103 nTPM
  • basal ganglia: 100 nTPM
  • spleen: 97 nTPM

Single-cell type

  • epididymal principal cells: 190 nCPM
  • epididymal efferent duct absorptive cells: 131 nCPM
  • gastric chief cells: 131 nCPM
  • enteric transient amplifying cells: 125 nCPM
  • epididymal efferent duct ciliated cells: 125 nCPM
  • enteric stem cells: 114 nCPM

Immune cell

  • plasmacytoid DC: 484 nTPM
  • total PBMC: 461 nTPM
  • intermediate monocyte: 409 nTPM
  • myeloid DC: 388 nTPM
  • non-classical monocyte: 387 nTPM
  • classical monocyte: 379 nTPM

Brain region

  • hypothalamus: 51 nTPM
  • cerebral cortex: 48 nTPM
  • thalamus: 46 nTPM
  • basal ganglia: 44 nTPM
  • pons: 43 nTPM
  • white matter: 43 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)
1.86
gnomAD pLI
0
DepMap mean gene effect
-0.12
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

Antibody and autoantibody relevanceSeroatlas analysis

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

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

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