Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Gene tree
  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Syp ENSRNOG00000059720

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Description

synaptophysin [Source:RGD Symbol;Acc:3802]

Gene Synonyms

Syp1

Location

Primary_assembly X: 17,521,348-17,536,984 reverse strand.

GRCr8:CM070411.1

About this gene

This gene has 2 transcripts (splice variants), 265 orthologues, 3 paralogues and is associated with 22 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000107562.2	Syp-202	2892	425aa	ENSRNOP00000096197.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AQE3	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,
ENSRNOT00000085907.3	Syp-201	2333	304aa	ENSRNOP00000075360.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2KAD8	-

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Summary

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