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: EGLN1 ENSOCUG00000013221

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Description

egl-9 family hypoxia inducible factor 1 [Source:HGNC Symbol;Acc:HGNC:1232]

Location

Chromosome 16: 36,569,377-36,619,245 forward strand.

OryCun2.0:CM000805.1

About this gene

This gene has 2 transcripts (splice variants), 229 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000013223.3	EGLN1-202	2740	457aa	ENSOCUP00000011383.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1T4Z3	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,
ENSOCUT00000034097.2	EGLN1-201	2387	436aa	ENSOCUP00000027146.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	U3KPI6	-

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Summary

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