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
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Syt4 ENSRNOG00000017333

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Description

synaptotagmin 4 [Source:RGD Symbol;Acc:68397]

Location

Primary_assembly 18: 23,312,859-23,320,815 reverse strand.

GRCr8:CM070408.1

About this gene

This gene has 2 transcripts (splice variants), 204 orthologues, 31 paralogues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000023594.7	Syt4-201	1982	425aa	ENSRNOP00000023593.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J2N4 P50232	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,
ENSRNOT00000110395.2	Syt4-202	1756	413aa	ENSRNOP00000097035.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AR88	-

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Summary

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