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: Exosc5 ENSRNOG00000020635

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Description

exosome component 5 [Source:RGD Symbol;Acc:1307861]

Gene Synonyms

LOC308441

Location

Primary_assembly 1: 90,293,797-90,305,046 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 186 orthologues, 2 paralogues and is associated with 9 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000094608.2	Exosc5-203	1063	270aa	ENSRNOP00000089044.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GHQ8	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,
ENSRNOT00000094088.2	Exosc5-202	901	215aa	ENSRNOP00000094450.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GL66	-
ENSRNOT00000028026.7	Exosc5-201	894	219aa	ENSRNOP00000028026.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AB24 F1LSX7	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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