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: rxrbb ENSDARG00000002006

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Description

retinoid x receptor, beta b [Source:NCBI gene;Acc:30486]

Gene Synonyms

NR2B2-B, rxrd, unp286

Location

Chromosome 16: 18,534,834-18,572,875 forward strand.

GRCz11:CM002900.2

About this gene

This gene has 3 transcripts (splice variants), 211 orthologues and 19 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000021596.9	rxrbb-201	1573	422aa	ENSDARP00000022973.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B3DG77	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,
ENSDART00000180168.1	rxrbb-203	6341	422aa	ENSDARP00000145278.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B3DG77	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,
ENSDART00000147844.2	rxrbb-202	732	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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