Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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 ENSOCUG00000023222

.

Description

egl-9 family hypoxia inducible factor 2 [Source:UniProtKB Gene Name;Acc:A0A5F9CJW6]

Location

Scaffold GL018789: 1,007,414-1,015,358 reverse strand.

About this gene

This gene has 4 transcripts (splice variants), 191 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000049094.1	EGLN2-204	2341	501aa	ENSOCUP00000039399.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5F9D1Z2	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,
ENSOCUT00000045346.1	EGLN2-201	2312	438aa	ENSOCUP00000034848.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5F9CMI7	-
ENSOCUT00000023652.3	EGLN2-203	1967	403aa	ENSOCUP00000018118.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1TMB0	-
ENSOCUT00000050244.1	EGLN2-202	1891	455aa	ENSOCUP00000033958.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5F9CJW6	-

.

Summary

.

.