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: NR2F1 ENSMODG00000020132

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Description

nuclear receptor subfamily 2 group F member 1 [Source:UniProtKB Gene Name;Acc:A0A5F8HHW8]

Location

Primary_assembly 3: 208,749,971-208,774,287 reverse strand.

ASM229v1:CM000370.1

About this gene

This gene has 3 transcripts (splice variants), 234 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSMODT00000062958.1	NR2F1-202	1545	415aa	ENSMODP00000059409.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5F8HHW8	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,
ENSMODT00000081839.1	NR2F1-201	1568	293aa	ENSMODP00000044568.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5F8GAN9	-
ENSMODT00000037620.3	NR2F1-203	1491	397aa	ENSMODP00000036031.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6SHM9	-

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Summary

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