Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
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Pathway
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External references
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ID History
- Gene history

Gene: EGLN3 ENSPRNG00000003643

Description

egl-9 family hypoxia inducible factor 3 [Ensembl NN prediction with score 100%]

Location

fParRan2.2:LR131973.1

About this gene

This gene has 1 transcript (splice variant).

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPRNT00000006670.1	EGLN3-201	1495	240aa	ENSPRNP00000006082.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6P7H827	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,

Summary