Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: EGLN2 ENSBTAG00000017996

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Description

egl-9 family hypoxia inducible factor 2 [Source:VGNC Symbol;Acc:VGNC:97265]

Location

Primary_assembly 18: 50,048,840-50,056,732 forward strand.

ARS-UCD1.3:CM008185.2

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
ENSBTAT00000072600.2	EGLN2-201	2081	435aa	ENSBTAP00000061162.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LUX2	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,
ENSBTAT00000023945.5	EGLN2-202	1973	399aa	ENSBTAP00000023945.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MX98	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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