Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
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: NR2F1 ENSMICG00000005642

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Description

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

Location

Chromosome 12: 86,276,837-86,288,475 reverse strand.

Mmur_3.0:CM007672.1

About this gene

This gene has 3 transcripts (splice variants), 228 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSMICT00000058465.1	NR2F1-201	4115	422aa	ENSMICP00000041854.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8B7FFY9	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,
ENSMICT00000005641.3	NR2F1-202	1197	398aa	ENSMICP00000005147.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C5UQR6	-
ENSMICT00000049850.2	NR2F1-203	822	273aa	ENSMICP00000035069.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C5W770	-

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Summary

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