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

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Gene: aplnr2 ENSDARG00000004447

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Description

apelin receptor 2 [Source:NCBI gene (formerly Entrezgene);Acc:793710]

Location

Chromosome 7: 38,685,545-38,689,562 reverse strand.

GRCz11:CM002891.2

About this gene

This gene has 2 transcripts (splice variants), 173 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000167209.3	aplnr2-202	2250	408aa	ENSDARP00000133169.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QJG4	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,
ENSDART00000074490.5	aplnr2-201	1278	408aa	ENSDARP00000068978.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QJG4	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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