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: EIF2AK1 ENSSSCG00000007592

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Description

eukaryotic translation initiation factor 2 alpha kinase 1 [Source:VGNC Symbol;Acc:VGNC:87606]

Location

Primary_assembly 3: 5,075,054-5,113,622 forward strand.

Sscrofa11.1:CM000814.5

About this gene

This gene has 3 transcripts (splice variants), 208 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000008332.5	EIF2AK1-201	1963	633aa	ENSSSCP00000008113.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1RFM6	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,
ENSSSCT00000069652.1	EIF2AK1-203	6636	604aa	ENSSSCP00000065384.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QKM4 A0A8D0YGQ8	-
ENSSSCT00000089039.1	EIF2AK1-202	6631	630aa	ENSSSCP00000060447.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2Q942 A0A8D0YGA2	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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