Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
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: Becn2 ENSRNOG00000038076

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Description

beclin 2 [Source:RGD Symbol;Acc:1563293]

Gene Synonyms

LOC289269, RGD1563293

Location

Primary_assembly 13: 87,844,531-87,845,787 forward strand.

mRatBN7.2:CM026986.1

About this gene

This gene has 1 transcript (splice variant), 181 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000057933.5	Becn2-201	1257	418aa	ENSRNOP00000054742.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M4I5	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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