Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- 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: NR2F1 ENSNLEG00000013901

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Description

nuclear receptor subfamily 2 group F member 1 [Source:HGNC Symbol;Acc:HGNC:7975]

Location

Chromosome 2: 107,753,010-107,765,971 forward strand.

Nleu_3.0:CM001648.1

About this gene

This gene has 3 transcripts (splice variants), 231 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSNLET00000048774.1	NR2F1-201	1269	422aa	ENSNLEP00000041574.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3HD61	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,
ENSNLET00000017723.3	NR2F1-203	1740	263aa	ENSNLEP00000016870.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1RUE4	-
ENSNLET00000052069.1	NR2F1-202	1194	397aa	ENSNLEP00000028568.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3GBB6	-

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Summary

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