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: Syt10 ENSRNOG00000014296

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Description

synaptotagmin 10 [Source:RGD Symbol;Acc:62041]

Gene Synonyms

sytX

Location

Primary_assembly 7: 120,862,972-120,920,863 reverse strand.

mRatBN7.2:CM026980.1

About this gene

This gene has 2 transcripts (splice variants), 217 orthologues, 31 paralogues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000098923.1	Syt10-202	1747	523aa	ENSRNOP00000091005.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	O08625	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,
ENSRNOT00000019406.4	Syt10-201	1696	520aa	ENSRNOP00000019406.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QAR7	-

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Summary

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