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

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Gene: SYN3 ENSSSCG00000040453

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Description

synapsin III [Source:HGNC Symbol;Acc:HGNC:11496]

Location

Primary_assembly 5: 12,473,793-12,500,076 forward strand.

Sscrofa11.1:CM000816.5

About this gene

This gene has 2 transcripts (splice variants), 213 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000000165.5	SYN3-202	2006	335aa	ENSSSCP00000000163.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1SPS2	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,
ENSSSCT00000051918.3	SYN3-201	1982	327aa	ENSSSCP00000042520.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AFB0 A0A8D0LLP3	-

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Summary

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