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
External references
Supporting evidence
ID History
- Gene history

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Gene: Eif1b ENSRNOG00000018848

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Description

eukaryotic translation initiation factor 1B [Source:RGD Symbol;Acc:1309241]

Gene Synonyms

LOC301068, RGD1309241

Location

Primary_assembly 8: 129,078,293-129,083,772 forward strand.

GRCr8:CM070398.1

About this gene

This gene has 2 transcripts (splice variants), 157 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000109763.2	Eif1b-202	805	132aa	ENSRNOP00000078643.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZL75	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,
ENSRNOT00000025615.9	Eif1b-201	502	113aa	ENSRNOP00000025615.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B5DFN1 F7F4Q4	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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Paralogues

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