Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: EGLN3 ENSPSNG00000018355

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Description

egl-9 family hypoxia inducible factor 3 [Source:UniProtKB Gene Name;Acc:A0A8C9CT17]

Location

Primary_assembly 2: 112,997,390-113,026,032 reverse strand.

mPhoSin1.pri:CM018157.1

About this gene

This gene has 2 transcripts (splice variants), 203 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPSNT00000028349.1	EGLN3-201	2613	239aa	ENSPSNP00000025215.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C9CHU1	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,
ENSPSNT00000028366.1	EGLN3-202	5221	119aa	ENSPSNP00000025232.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C9CT17	-

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Summary

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