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 ENSAMEG00000023682

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Description

egl-9 family hypoxia inducible factor 3 [Source:NCBI gene (formerly Entrezgene);Acc:100470632]

Location

Primary_assembly 20: 11,838,971-11,865,175 reverse strand.

ASM200744v2:CM022838.1

About this gene

This gene has 2 transcripts (splice variants), 205 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSAMET00000031276.1	EGLN3-201	2175	239aa	ENSAMEP00000029251.1	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,
ENSAMET00000044768.1	EGLN3-202	2175	158aa	ENSAMEP00000035489.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-

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Summary

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