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

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Gene: egln2 ENSDARG00000062562

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Description

egl-9 family hypoxia inducible factor 2 [Source:HGNC Symbol;Acc:HGNC:14660]

Location

Chromosome 15: 8,335,600-8,382,997 forward strand.

GRCz11:CM002899.2

About this gene

This gene has 2 transcripts (splice variants), 191 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000152603.2	egln2-201	3438	464aa	ENSDARP00000126905.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7F8S1	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,
ENSDART00000190066.1	egln2-202	1971	464aa	ENSDARP00000152746.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7F8S1	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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