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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: EGLN1 ENSXETG00000021414

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Description

egl-9 family hypoxia-inducible factor 1 [Source:Xenbase;Acc:XB-GENE-1017116]

Location

Primary_assembly 5: 57,917,082-57,955,273 forward strand.

UCB_Xtro_10.0:CM004447.2

About this gene

This gene has 2 transcripts (splice variants), 231 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSXETT00000106496.1	EGLN1-201	2862	396aa	ENSXETP00000106518.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A803JF27	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,
ENSXETT00000046302.5	EGLN1-202	2584	394aa	ENSXETP00000046302.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q28E59	-

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Summary

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