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

Configure this page

Share this page

Bookmark this page

.

Gene: EGLN2 ENSMODG00000007965

.

Description

egl-9 family hypoxia inducible factor 2 [Source:NCBI gene;Acc:100018431]

Location

Primary_assembly 4: 384,896,068-384,904,400 forward strand.

ASM229v1:CM000371.1

About this gene

This gene has 2 transcripts (splice variants), 195 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSMODT00000010102.3	EGLN2-202	1218	396aa	ENSMODP00000009910.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7DRH1	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,
ENSMODT00000077771.1	EGLN2-201	1830	388aa	ENSMODP00000053182.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

.

Summary

.

.