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

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Gene: Syt9 ENSRNOG00000019613

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Description

synaptotagmin 9 [Source:RGD Symbol;Acc:621169]

Gene Synonyms

Sytv

Location

Primary_assembly 1: 161,275,734-161,455,007 forward strand.

mRatBN7.2:CM026974.1

About this gene

This gene has 2 transcripts (splice variants), 278 orthologues, 31 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000026607.6	Syt9-201	1437	449aa	ENSRNOP00000026607.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QF44	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,
ENSRNOT00000119170.1	Syt9-202	2534	448aa	ENSRNOP00000083409.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZX57	-

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Summary

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