Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: EIF5A ENSBTAG00000002018

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Description

eukaryotic translation initiation factor 5A [Source:NCBI gene (formerly Entrezgene);Acc:444990]

Location

Primary_assembly 19: 27,015,093-27,020,473 forward strand.

ARS-UCD2.0:CM008186.2

About this gene

This gene has 2 transcripts (splice variants), 221 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000094840.2	EIF5A-202	1181	199aa	ENSBTAP00000081787.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6EWQ7	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, APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2,
ENSBTAT00000084447.3	EIF5A-201	1194	183aa	ENSBTAP00000069104.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF7AHP7	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2,

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Summary

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