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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Akt2 ENSRNOG00000018677

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Description

AKT serine/threonine kinase 2 [Source:RGD Symbol;Acc:2082]

Location

Primary_assembly 1: 92,014,859-92,061,420 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 255 orthologues, 5 paralogues and is associated with 37 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000025303.5	Akt2-201	3337	495aa	ENSRNOP00000025303.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7EKK8	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,
ENSRNOT00000105853.2	Akt2-202	3166	438aa	ENSRNOP00000078809.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZLJ3	-
ENSRNOT00000118840.2	Akt2-203	2740	473aa	ENSRNOP00000095075.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y943 A0A8I6ASU3	-

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data