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 ENSMICG00000000618

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Description

egl-9 family hypoxia inducible factor 3 [Source:HGNC Symbol;Acc:HGNC:14661]

Location

Chromosome 3: 63,910,998-63,937,776 forward strand.

Mmur_3.0:CM007663.1

About this gene

This gene has 3 transcripts (splice variants), 204 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSMICT00000000617.3	EGLN3-202	768	255aa	ENSMICP00000000554.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C5XAW2	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,
ENSMICT00000040772.2	EGLN3-201	4034	239aa	ENSMICP00000033045.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8B7GYT7	-
ENSMICT00000064028.1	EGLN3-203	420	140aa	ENSMICP00000050064.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C5YFR1	-

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Summary

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