SelenoDB
Release 2.0
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Gene Report for SPG00001415_2.0
Identity
GeneSelenoprotein N (SELENON)
SpeciesMonodelphis domestica (Opossum)
DescriptionUnknown function. Mutations in this gene cause the classical phenotype of multiminicore disease and congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome. (NCBI)
FamilySelenoprotein N
Synonyms Selenoprotein N (SelN)
Selenoprotein N (SEPN)
SubfamilyNone
SynonymsNone
Gene IDSPG00001415
Gene release2.0
External IDNone
Annotation
Prediction method(s)
Promoter prediction (5000bp upstream, N/A) [Report annotation error]
(Selenoprofiles, Ensembl 68) [Report annotation error]
Conceptual translation (Translate, Standard code with Sec) [Report annotation error]
OrientationForward
Structure gene structure

FeatureCol PromoterCol Coding exonCol Non coding exon (UTR)Col IntronCol SECIS
ResidueCol SecCol Cys or Other

Gene
Transcript(s) Promoter(s) Protein(s) Secis
SPT00001511_2.0SPR00001576_2.0SPP00001519_2.0N/A
Sequence
Sequence SEQ00001414_2.0
External IDNone
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