Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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Ontologies
Phenotypes
Genetic Variation
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- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
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ID History
- Gene history

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Gene: Fxn ENSRNOG00000015213

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Description

frataxin [Source:RGD Symbol;Acc:1565754]

Gene Synonyms

LOC499335, RGD1565754

Location

Primary_assembly 1: 221,872,420-221,897,540 reverse strand.

mRatBN7.2:CM026974.1

About this gene

This gene has 1 transcript (splice variant), 217 orthologues and is associated with 9 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000071614.3	Fxn-201	2151	208aa	ENSRNOP00000066555.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RAK4	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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