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: FOXR1 ENSPTRG00000004358

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Description

forkhead box R1 [Source:VGNC Symbol;Acc:VGNC:1056]

Location

Chromosome 11: 119,437,107-119,446,780 forward strand.

Pan_tro_3.0:CM000325.3

About this gene

This gene has 1 transcript (splice variant), 83 orthologues and 39 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000008092.3	FOXR1-201	1242	292aa	ENSPTRP00000007469.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2X5L9 H2Q4X1	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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