Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Gene: AAR2 ENSPTRG00000013456

Description

AAR2 splicing factor [Source:VGNC Symbol;Acc:VGNC:9819]

Location

Pan_tro_3.0:CM000334.4

About this gene

This gene has 2 transcripts (splice variants) and 194 orthologues.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000058105.3	AAR2-202	1197	398aa	ENSPTRP00000051050.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XB86 H2R813	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,
ENSPTRT00000025020.5	AAR2-201	3047	384aa	ENSPTRP00000023096.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XSK0 H2QKA2	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