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

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Gene: eif1axa ENSDARG00000029003

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Description

eukaryotic translation initiation factor 1A X-linked a [Source:NCBI gene (formerly Entrezgene);Acc:450062]

Gene Synonyms

eif1ax, zgc:101670

Location

Chromosome 5: 24,002,598-24,008,997 reverse strand.

GRCz11:CM002889.2

About this gene

This gene has 1 transcript (splice variant), 316 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000066645.5	eif1axa-201	950	144aa	ENSDARP00000066644.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5XJR0	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 P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Summary

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