Gene
AKT3
AKT serine/threonine kinase 3
- HGNC 393↗(opens in a new tab)
- Ensembl gene ENSG00000117020↗(opens in a new tab)
- NCBI Gene 10000↗(opens in a new tab)
Summary
- Cytogenetic location
- 1q43-q44
- Coordinates
- Chromosome 1: 243,499,724–243,850,243 (GRCh38)
- Exons
- 14 exons across 350.5 kb
- Protein
- 479 amino acids
- Also known as
- PKBG, RAC-gamma, PRKBG
- MANE Select transcript
- ENST00000673466.1NM_005465.7
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read AKT3, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated reports relevant to this gene
No Genome Test report reads AKT3 yet. The test sequences your whole genome, so your data includes it all the same.
How AKT3 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 7.3 kb of the gene's 350.5 kb; 1,440 of those bases code for the protein.
How a genome test reads AKT3
9
positions in AKT3 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 350.5 kb of AKT3, introns included, not only the 7.3 kb of exons.
Traits linked to AKT3
The Human Phenotype Ontology lists these as features of the rare conditions AKT3 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Hemimegalencephaly
- Enlarged brain
- Epilepsy
- Hyperintensity of cerebral white matter on MRI
- Interictal EEG abnormality
- More grooves in brain
- Too much cerebrospinal fluid in the brain
- EEG with burst suppression
Show 22 more traits
- EEG with focal sharp slow waves
- EEG with focal spikes
- EEG with polyspike wave complexes
- Focal cortical dysplasia
- Focal motor seizure
- Global developmental delay
- Hemihypsarrhythmia
- Ventriculomegaly
- Abnormal neuron shape
- Cranial nerve paralysis
- Epileptic spasm
- Fewer and broader ridges in brain
- Focal tonic seizure
- Gliosis
- Gray matter heterotopia
- Intellectual disability, severe
- Jerking
- Repeated seizures without recovery between them
- Sudden loss of muscle tone
- Weakness of one side of body
- Intellectual disability
- Underdevelopment of part of brain called corpus callosum
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). AKT3 gene: AKT serine/threonine kinase 3. Retrieved 17 October 2026, from https://dantelabs.com/genes/akt3
Dante Labs. AKT3 gene: AKT serine/threonine kinase 3 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/akt3
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks