Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: selenot2 ENSDARG00000023220

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Description

selenoprotein T, 2 [Source:NCBI gene;Acc:352917]

Gene Synonyms

cb699, fj34h11, selt2, sept2, wu:fj34h11, zgc:112046

Location

Chromosome 14: 17,580,571-17,588,345 reverse strand.

GRCz11:CM002898.2

About this gene

This gene has 3 transcripts (splice variants), 69 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000143486.3	selenot2-203	1650	210aa	ENSDARP00000114858.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q502K9	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSDART00000065002.7	selenot2-201	798	149aa	ENSDARP00000065001.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7F4Y1	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000132394.3	selenot2-202	312	100aa	ENSDARP00000133857.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0R4IJF1	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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