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: EGLN3 ENSBMUG00000008216

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Description

egl-9 family hypoxia inducible factor 3 [Source:NCBI gene;Acc:102280498]

Location

Primary_assembly JH881433.1: 341,384-369,784 forward strand.

About this gene

This gene has 2 transcripts (splice variants), 207 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBMUT00000012353.1	EGLN3-202	2318	248aa	ENSBMUP00000010634.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSBMUT00000012351.1	EGLN3-201	1412	239aa	ENSBMUP00000010633.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	L8IFR3	-

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Summary

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