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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: NR2E1 ENSPTRG00000018472

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Description

nuclear receptor subfamily 2 group E member 1 [Source:VGNC Symbol;Acc:VGNC:3597]

Location

Chromosome 6: 111,649,656-111,672,355 forward strand.

Pan_tro_3.0:CM000320.3

About this gene

This gene has 2 transcripts (splice variants), 225 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000105131.1	NR2E1-202	3812	422aa	ENSPTRP00000073105.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3S7T8 A0A6D2XD46	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,
ENSPTRT00000034137.4	NR2E1-201	3189	385aa	ENSPTRP00000031550.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2YAH3 H2QTI2	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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