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: stx8 ENSDARG00000103173

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Description

syntaxin 8 [Source:NCBI gene (formerly Entrezgene);Acc:393346]

Location

Chromosome 6: 19,689,464-19,802,580 forward strand.

GRCz11:CM002890.2

About this gene

This gene has 2 transcripts (splice variants), 185 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000164960.2	stx8-201	1365	235aa	ENSDARP00000139377.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q7T361	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,
ENSDART00000168031.2	stx8-202	825	54aa	ENSDARP00000132359.1	Nonsense mediated decay	-	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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