Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: Insyn2b ENSRNOG00000032329

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Description

inhibitory synaptic factor family member 2B [Source:RGD Symbol;Acc:2320105]

Gene Synonyms

AABR07029269.1, Fam196b, LOC100361460

Location

Primary_assembly 10: 19,507,084-19,511,298 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 1 transcript (splice variant), 125 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000050610.4	Insyn2b-201	2616	489aa	ENSRNOP00000049022.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZZH5	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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