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 LSLocalizationUniProt · 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
- Selenoprotein, Rdx-type
- Thioredoxin-like superfamily
- Rdx family
- Selenoprotein SelWTH-like
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.
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