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

Configure this page

Share this page

Bookmark this page

.

Gene: RAI2 ENSSSCG00000012153

.

Description

retinoic acid induced 2 [Source:VGNC Symbol;Acc:VGNC:92069]

Location

Primary_assembly X: 14,244,317-14,309,143 reverse strand.

Sscrofa11.1:CM000830.5

About this gene

This gene has 2 transcripts (splice variants), 169 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000076885.2	RAI2-202	3965	665aa	ENSSSCP00000065773.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QMC9 A0A8D0TI62	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,
ENSSSCT00000013294.2	RAI2-201	2213	531aa	ENSSSCP00000012938.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1DH91 F1SQQ4	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

.

.