Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: nr2f6a ENSDARG00000003607

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Description

nuclear receptor subfamily 2, group F, member 6a [Source:ZFIN;Acc:ZDB-GENE-030131-4362]

Gene Synonyms

COUP(II), EAR2-A, couptf2, fc94g11, wu:fc94g11, zgc:77259

Location

Chromosome 2: 24,374,305-24,386,382 forward strand.

GRCz11:CM002886.2

About this gene

This gene has 3 transcripts (splice variants), 214 orthologues and 19 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000022379.9	nr2f6a-201	2912	402aa	ENSDARP00000009513.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6P117	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,
ENSDART00000133818.2	nr2f6a-202	800	88aa	ENSDARP00000119818.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0UXT4	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSDART00000135323.2	nr2f6a-203	729	243aa	ENSDARP00000115445.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QA67	5' and 3' truncations in transcript evidence prevent annotation of the start and the end of the CDS.CDS 5' and 3' incomplete,

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Summary

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