Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
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: Syndig1 ENSRNOG00000031536

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Description

synapse differentiation inducing 1 [Source:RGD Symbol;Acc:1310753]

Gene Synonyms

DSPC2, LOC103691925, LOC362235, RGD1310753, Tmem90b

Location

Primary_assembly 3: 158,491,996-158,658,652 forward strand.

GRCr8:CM070393.1

About this gene

This gene has 1 transcript (splice variant), 130 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000068210.5	Syndig1-201	2320	258aa	ENSRNOP00000060788.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6K7G0 Q58DZ9	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,

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Summary

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