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

Configure this page

Share this page

Bookmark this page

.

Gene: SELENOV ENSSSCG00000002986

.

Description

selenoprotein V [Source:NCBI gene (formerly Entrezgene);Acc:100307053]

Gene Synonyms

SELV

Location

Primary_assembly 6: 48,162,428-48,167,437 forward strand.

Sscrofa11.1:CM000817.5

About this gene

This gene has 2 transcripts (splice variants), 44 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000003317.3	SELENOV-201	1216	342aa	ENSSSCP00000003235.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1RHD7	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,
ENSSSCT00000101433.1	SELENOV-202	1143	331aa	ENSSSCP00000079904.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8W4FKP5	-

.

Summary

.

.