Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Exosc2 ENSRNOG00000009245

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Description

exosome component 2 [Source:RGD Symbol;Acc:1306573]

Gene Synonyms

LOC366017

Location

Primary_assembly 3: 35,360,666-35,371,373 forward strand.

GRCr8:CM070393.1

About this gene

This gene has 2 transcripts (splice variants), 209 orthologues, 1 paralogue and is associated with 9 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000012312.8	Exosc2-201	1896	293aa	ENSRNOP00000012311.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JU28 D3ZBP3	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,
ENSRNOT00000093692.3	Exosc2-202	975	240aa	ENSRNOP00000076582.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y5D3	-

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Paralogues

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