Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: EGLN2 ENSCAFG00000005079

.

Description

egl-9 family hypoxia inducible factor 2 [Source:VGNC Symbol;Acc:VGNC:97191]

Location

Primary_assembly 1: 112,395,201-112,404,253 reverse strand.

Dog10K_Boxer_Tasha:CM000001.4

About this gene

This gene has 2 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSCAFT00000008170.5	EGLN2-201	2152	405aa	ENSCAFP00000007568.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C0S558 A0A8I3N3U4	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,
ENSCAFT00000083939.2	EGLN2-202	2051	396aa	ENSCAFP00000048609.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C0S593 A0A8I3MME9	-

.

Summary

.

.