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

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Gene: rx2 ENSDARG00000040321

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Description

retinal homeobox gene 2 [Source:ZFIN;Acc:ZDB-GENE-990415-237]

Location

Chromosome 2: 55,833,425-55,861,351 reverse strand.

GRCz11:CM002886.2

About this gene

This gene has 2 transcripts (splice variants), 122 orthologues, 56 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000059003.6	rx2-201	1489	327aa	ENSDARP00000059002.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QNV0	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,
ENSDART00000122576.3	rx2-202	1138	327aa	ENSDARP00000105437.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QNV0	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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