Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: Nr2e1 ENSRNOG00000050550

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Description

nuclear receptor subfamily 2, group E, member 1 [Source:RGD Symbol;Acc:1595162]

Gene Synonyms

LOC684085, TLX

Location

Primary_assembly 20: 47,632,347-47,653,464 reverse strand.

GRCr8:CM070410.1

About this gene

This gene has 2 transcripts (splice variants), 229 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000075151.3	Nr2e1-201	3140	385aa	ENSRNOP00000064408.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZSJ5 A6K6Y5 M0R4V9	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,
ENSRNOT00000106191.2	Nr2e1-202	1816	173aa	ENSRNOP00000093877.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AJN9	-

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Summary

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