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
External references
Supporting evidence
ID History
- Gene history

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Gene: EGLN2 ENSPTRG00000011010

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Description

egl-9 family hypoxia inducible factor 2 [Source:VGNC Symbol;Acc:VGNC:14743]

Location

Chromosome 19: 42,851,593-42,860,037 forward strand.

Pan_tro_3.0:CM000333.3

About this gene

This gene has 1 transcript (splice variant), 195 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000020431.6	EGLN2-201	2073	407aa	ENSPTRP00000044177.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G2HG38	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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