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

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Gene: RAI2 ENSOCUG00000026517

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Description

retinoic acid induced 2 [Source:HGNC Symbol;Acc:HGNC:9835]

Location

Chromosome X: 3,721,713-3,781,506 reverse strand.

OryCun2.0:CM000811.1

About this gene

This gene has 1 transcript (splice variant), 169 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000023934.2	RAI2-201	1604	501aa	ENSOCUP00000021662.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1TX62	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,

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Summary

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