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

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Gene: RAX2 ENSPTRG00000010277

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Description

retina and anterior neural fold homeobox 2 [Source:VGNC Symbol;Acc:VGNC:2273]

Location

Chromosome 19: 3,932,355-3,936,074 reverse strand.

Pan_tro_3.0:CM000333.3

About this gene

This gene has 1 transcript (splice variant), 55 orthologues and 58 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000018872.5	RAX2-201	2740	184aa	ENSPTRP00000017466.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8JQR0 A2T711	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,

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Summary

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