Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- 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: Perm1 ENSRNOG00000020244

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Description

PPARGC1 and ESRR induced regulator, muscle 1 [Source:RGD Symbol;Acc:1304931]

Gene Synonyms

LOC313776, RGD1304931

Location

Primary_assembly 5: 172,082,249-172,087,542 forward strand.

GRCr8:CM070395.1

About this gene

This gene has 1 transcript (splice variant), 114 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000027476.7	Perm1-201	3861	788aa	ENSRNOP00000027476.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IUW7 D3ZH76	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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