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 ENSPPYG00000010005

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Description

egl-9 family hypoxia inducible factor 2 [Source:NCBI gene (formerly Entrezgene);Acc:100172704]

Location

Primary_assembly 19: 38,796,164-38,825,519 forward strand.

Susie_PABv2:CM009281.2

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
ENSPPYT00000056876.1	EGLN2-201	2106	418aa	ENSPPYP00000038059.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5YP22	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,
ENSPPYT00000011637.2	EGLN2-202	2391	407aa	ENSPPYP00000011199.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2NYW6	-

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Summary

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