SELENOH - selenoprotein H Gene
Also Known as SELH; C11orf31; C17orf10
Species: Homo sapiens
About SELENOH
This gene has 6 transcripts (splice variants) and 49 orthologues. Ubiquitous expression in adrenal (RPKM 17.7), spleen (RPKM 16.5) and 25 other tissues.
Summary
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]
SELENOH Products (2)
| mRNA | Protein | Name |
|---|---|---|
| NM_001321335.2 | NP_001308264.1 | selenoprotein H |
| NM_170746.4 | NP_734467.1 | selenoprotein H |
SELENOH Protein Structure
Rdx: Rdx family (35 - 119)
- 0
- 100
- 122 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
selenoprotein H |
|
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Spina Bifida Occulta |
|
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| Neural Tube Defects |
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| Anencephaly |
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