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

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Gene: RGR ENSBTAG00000015681

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Description

retinal G protein coupled receptor [Source:VGNC Symbol;Acc:VGNC:33909]

Location

Primary_assembly 28: 39,202,110-39,227,365 forward strand.

ARS-UCD2.0:CM008195.2

About this gene

This gene has 3 transcripts (splice variants), 267 orthologues and 25 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000104167.2	RGR-201	1384	306aa	ENSBTAP00000080602.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S5V8	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,
ENSBTAT00000020822.8	RGR-203	1368	287aa	ENSBTAP00000020822.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	P47803	-
ENSBTAT00000096382.2	RGR-202	801	253aa	ENSBTAP00000100326.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TPJ6	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,

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Summary

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