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

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Gene: Syt8 ENSRNOG00000020245

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Description

synaptotagmin 8 [Source:RGD Symbol;Acc:68399]

Location

Primary_assembly 1: 207,017,461-207,023,076 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 174 orthologues, 31 paralogues and is associated with 7 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000150736.1	Syt8-202	1600	395aa	ENSRNOP00000108224.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000027454.7	Syt8-201	1282	395aa	ENSRNOP00000027454.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HY46 F1LQ42	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,

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Summary

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