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  2. SELENOH - selenoprotein H Gene

SELENOH - selenoprotein H Gene

Homo sapiens

Also known as SELH; C11orf31; C17orf10

Gene ID: 280636 | Gene type: protein coding

About SELENOH

Cytogenetic location: 11q12.1 Genomic coordinates (GRCh38): 11:57,741,491-57,743,550 (from NCBI)

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: Rdx family (35 - 119)

  • 0
  • 100
  • 122 a.a.
Protein Preferred Names Protein Names

selenoprotein H

Related Diseases

Diseases Alias
Spina Bifida Occulta
Neural Tube Defects

Spina Bifida

Neural Tube Defect

NTD

Neural Tube Defects, Susceptibility To

Spinal Dysraphism

Spina Bifida, Susceptibility To

Rachischisis

Cleft Spine

Open Spine

Hydrocele Spinalis

Neural Tube Defect Nos

Sb - [Spina Bifida]

Spinal Hernia Nos

Spinal Fissure Nos

Anencephaly

Aprosencephaly

Anencephalus

Congenital Absence Of Brain

Absence Of A Large Part Of The Brain And The Skull

Anencephalia

Anencephalic Monster

Brain Absence

Brain Agenesis

Brain Aplasia

Absent Brain

Anencephalic

Congenital Absence Of Cerebrum

Congenital Hemicrania

Incomplete Anencephaly

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta SELENOH VGNC VGNC:82234
Felis catus SELENOH VGNC VGNC:81942
Mus musculus SELENOH MGD MGI:1919907
Rattus norvegicus SELENOH RGD RGD:1563348