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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: SELV ENSG00000186838

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Description

Selenoprotein V [Source:UniProtKB/Swiss-Prot;Acc:P59797]

Location

Chromosome 19: 40,005,753-40,011,326 forward strand.

GRCh37:CM000681.1

About this gene

This gene has 4 transcripts (splice variants), 44 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000335426.4	SELV-001	1704	346aa	ENSP00000333956.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS54266	P59797	NM_182704.1	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, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENST00000423711.1	SELV-201	1704	346aa	ENSP00000412508.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		C9IZ47	-	A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENST00000600586.1	SELV-002	481	73aa	ENSP00000470671.1	Nonsense mediated decay		-	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENST00000597876.1	SELV-003	645	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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