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

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Gene: eif3eb ENSDARG00000002549

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Description

eukaryotic translation initiation factor 3, subunit E, b [Source:NCBI gene;Acc:561049]

Gene Synonyms

eif3s6b, im:7147439

Location

Chromosome 19: 22,622,355-22,664,398 reverse strand.

GRCz11:CM002903.2

About this gene

This gene has 5 transcripts (splice variants), 216 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000023926.11	eif3eb-201	3883	446aa	ENSDARP00000003276.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QHS3	APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5,
ENSDART00000136295.4	eif3eb-203	1679	439aa	ENSDARP00000120794.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	T1ECV8	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,
ENSDART00000135651.3	eif3eb-202	1895	401aa	ENSDARP00000118894.1	Nonsense mediated decay	Z4YIU6	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,
ENSDART00000150189.2	eif3eb-205	754	63aa	ENSDARP00000123842.1	Nonsense mediated decay	F8W4Y6	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000150052.3	eif3eb-204	697	91aa	ENSDARP00000124720.1	Nonsense mediated decay	F8W2I2	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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