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 ENSMODG00000017625

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Description

egl-9 family hypoxia inducible factor 3 [Source:NCBI gene;Acc:100013679]

Location

Primary_assembly 1: 204,638,319-204,675,142 forward strand.

ASM229v1:CM000368.1

About this gene

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

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSMODT00000052749.1	EGLN3-202	735	244aa	ENSMODP00000056432.1	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,
ENSMODT00000022366.4	EGLN3-201	720	239aa	ENSMODP00000021979.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6ZT25	-

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Summary

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