Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
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: EGLN2 ENSMICG00000028495

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Description

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

Location

Chromosome 22: 22,482,695-22,494,523 reverse strand.

Mmur_3.0:CM007682.1

About this gene

This gene has 2 transcripts (splice variants), 190 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSMICT00000036624.2	EGLN2-201	4856	405aa	ENSMICP00000025142.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8B7H3H8	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,
ENSMICT00000045727.2	EGLN2-202	2439	405aa	ENSMICP00000021168.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8B7H3H8	-

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Summary

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