Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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: egln1a ENSACLG00000023267

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Description

egl-9 family hypoxia-inducible factor 1a [Ensembl NN prediction with score 99.99%]

Location

Primary_assembly 13: 8,411,799-8,426,311 forward strand.

fAstCal1.3:LS420031.1

About this gene

This gene has 2 transcripts (splice variants), 212 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSACLT00000035166.2	egln1a-202	1578	125aa	ENSACLP00000034345.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3P8QXD1	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,
ENSACLT00000044714.1	egln1a-201	1459	110aa	ENSACLP00000066600.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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