Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: selenow2b ENSDARG00000089936

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Description

selenoprotein W, 2b [Source:NCBI gene (formerly Entrezgene);Acc:378438]

Gene Synonyms

cb696, sepw2b, si:dz180g5.2, zgc:123142, zgc:152839

Location

Chromosome 3: 20,103,746-20,106,233 reverse strand.

GRCz11:CM002887.2

About this gene

This gene has 2 transcripts (splice variants), 168 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000145285.3	selenow2b-202	1123	94aa	ENSDARP00000118513.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8M1PB21	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,
ENSDART00000135401.2	selenow2b-201	834	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript	-	-

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Summary

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