Entity Details

Primary name SELENON
Entity type gene
Source Source Link

Details

PrimaryID57190
RefseqGeneNG_009930
SymbolSELENON
Nameselenoprotein N
Chromosome1
Location1p36.11
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-09-02
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsSELN_HUMAN

GO terms

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GOName
GO:0005509 calcium ion binding
GO:0005789 endoplasmic reticulum membrane
GO:0016491 oxidoreductase activity
GO:0048741 skeletal muscle fiber development
GO:0055074 calcium ion homeostasis
GO:0060314 regulation of ryanodine-sensitive calcium-release channel activity
GO:1902884 positive regulation of response to oxidative stress

Diseases

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Disease IDSourceNameDescription
602771 OMIMRigid spine muscular dystrophy 1 (RSMD1)A neuromuscular disorder characterized by poor axial muscle strength, scoliosis and neck weakness, and a variable degree of spinal rigidity. Early ventilatory insufficiency can lead to death by respiratory failure. The disease is caused by variants affecting the gene represented in this entry.
255310 OMIMMyopathy, congenital, with fiber-type disproportion (CFTD)A genetically heterogeneous disorder in which there is relative hypotrophy of type 1 muscle fibers compared to type 2 fibers on skeletal muscle biopsy. However, these findings are not specific and can be found in many different myopathic and neuropathic conditions. The disease is caused by variants affecting the gene represented in this entry.