Gene: nr2f1b ENSDARG00000017168

Description

nuclear receptor subfamily 2, group F, member 1b [Source:NCBI gene (formerly Entrezgene);Acc:393564]

Location

GRCz11:CM002894.2

About this gene

This gene has 1 transcript (splice variant), 154 orthologues, 19 paralogues and is associated with 30 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000027242.6	nr2f1b-201	2786	389aa	ENSDARP00000010118.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6PH18-1	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,

Summary