> Trialight public data. Index of pages: https://trialight.com/llms.txt
> Web page: https://trialight.com/data/target/akt3-e83fd71b-7a8b-5c2d-b511-96cdd2ed530e
> Record changed: 2026-10-13

# AKT3

ENSG00000117020

Target class

Kinase

Chromosome

1

Approved drugs

1

Clinical candidates (approved and in development)

14

## Clinical evidence

**Approved drugs**

1

**ClinGen gene-disease validity**

Definitive

**Clinical candidates (approved and in development)**

14

## Druggability

**Chemical probe available**

Yes

## Names

**Target name**

AKT3

**Gene name**

AKT serine/threonine kinase 3

**Gene symbol**

AKT3

**Protein name**

RAC-gamma serine/threonine-protein kinase (EC 2.7.11.1) (Protein kinase Akt-3) (Protein kinase B gamma) (PKB gamma) (RAC-PK-gamma) (STK-2)

### Other names (3)

- PKBG
- RAC-gamma
- PRKBG

## Classification

**Gene biotype**

Protein coding

**Gene family**

Pleckstrin homology domain containing|AKT kinase family

**Target class**

Kinase

**Target type**

Human gene

## Expression and localisation

**Tissues expressed in**

54

**Protein localisation evidence grade**

Supported

**Highest tissue expression**

62.94

**Tissue specificity (Gini)**

0.378

**Tissue specificity (tau)**

0.677

## Pathways and interactions

**KEGG gene identifiers**

- hsa:10000

**Protein interaction confidence**

0.891073

**Protein interaction partners**

96

### Reactome pathways (29)

- R-HSA-111447
- R-HSA-1257604
- R-HSA-1358803
- R-HSA-165159
- R-HSA-165181
- R-HSA-198323
- R-HSA-198693
- R-HSA-199418
- R-HSA-211163
- R-HSA-389357
- R-HSA-389513
- R-HSA-392451
- R-HSA-5218920
- R-HSA-5628897
- R-HSA-5674400
- R-HSA-6804757
- R-HSA-6804758
- R-HSA-6804759
- R-HSA-69202
- R-HSA-69656
- R-HSA-8876198
- R-HSA-8941332
- R-HSA-8948751
- R-HSA-9607240
- R-HSA-9614399

And 4 more, listed on the interactive page.

## Genomic location

**End position**

243851079

**Start position**

243488233

**Chromosome**

1

**Strand**

Reverse

## Identifiers

**Ensembl gene ID**

ENSG00000117020

**HGNC ID**

HGNC:393

Source: [www.genenames.org](https://www.genenames.org/data/gene-symbol-report/#!/hgnc%5Fid/HGNC:393)

**NCBI Gene ID**

10000

**UniProt ID**

Q9Y243

## Cellular location

- Nucleus . Cytoplasm . Membrane
- Peripheral membrane protein . Note=Membrane-associated after cell stimulation leading to its translocation.
- Cytosol
- Golgi apparatus
- Nucleoplasm

### Publication evidence

- PubMed 20018949  
Source: [pubmed.ncbi.nlm.nih.gov](https://pubmed.ncbi.nlm.nih.gov/20018949/)

## Tissue expression

**Tissue specificity (tau)**

0.677012

**Expression inequality (Gini)**

0.378288

### Highest expression

Expression in transcripts per million

**Artery - Tibial**

62.94

**Uterus**

45.66

**Ovary**

45.65

**Fallopian Tube**

43.83

**Artery - Coronary**

42.7

### All tissues (54)

Expression in transcripts per million

- Artery - Tibial62.94
- Uterus45.66
- Ovary45.65
- Fallopian Tube43.83
- Artery - Coronary42.7
- Cervix - Ectocervix41.76
- Brain - Cerebellar Hemisphere41.61
- Artery - Aorta41.19
- Colon - Sigmoid37.01
- Cervix - Endocervix36.95
- Brain - Cerebellum36.11
- Nerve - Tibial35.86
- Esophagus - Muscularis33.27
- Esophagus - Gastroesophageal Junction31.93
- Bladder30.24
- Brain - Frontal Cortex (BA9)29.75
- Adipose - Subcutaneous28.93
- Lung24.91
- Thyroid24.39
- Breast - Mammary Tissue23.87
- Adipose - Visceral (Omentum)23.58
- Prostate23.13
- Cells - Cultured fibroblasts22.87
- Brain - Cortex22.33
- Pituitary21.73

And 29 more, listed on the interactive page.

## Biological functions

### Biological processes (7)

- GO:0001938  
Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/QuickGO/term/GO:0001938)
- GO:0007165  
Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/QuickGO/term/GO:0007165)
- GO:0010821  
Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/QuickGO/term/GO:0010821)
- GO:0043536  
Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/QuickGO/term/GO:0043536)
- GO:0090050  
Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/QuickGO/term/GO:0090050)
- GO:1905564  
Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/QuickGO/term/GO:1905564)
- GO:2000773  
Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/QuickGO/term/GO:2000773)

### Cellular components (2)

- GO:0005654  
Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/QuickGO/term/GO:0005654)
- GO:0005829  
Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/QuickGO/term/GO:0005829)

### Molecular functions (4)

- GO:0004672  
Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/QuickGO/term/GO:0004672)
- GO:0004674  
Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/QuickGO/term/GO:0004674)
- GO:0005515  
Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/QuickGO/term/GO:0005515)
- GO:0005524  
Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/QuickGO/term/GO:0005524)

## On-target safety

- heart disease  
### Studies

  - preclinical: Highly important for the heart and vasculature based on findings in genetically modified or kinase-inhibitor-treated mice. Role of kinase in heart/vasculature: Regulator of cardiomyocyte survival, growth and metabolism  
### Biological samples

  - cardiovascular system  
PubMed 21283106  
Source: [pubmed.ncbi.nlm.nih.gov](https://pubmed.ncbi.nlm.nih.gov/21283106/)

## Off-target safety

- regulation of catalytic activity  
### Studies

  - biochemical: NVS\_ENZ\_hAKT3, is one of one assay component(s) measured or calculated from the NVS\_ENZ\_hAKT3 assay. It is designed to make measurements of enzyme activity, a form of enzyme reporter, as detected with fluorescence intensity signals by Fluorescence and electrophoretic mobility shift technology.  
### Biological samples

  - cell-free  
Evidence source  
Source: [www.epa.gov](https://www.epa.gov/chemical-research/exploring-toxcast-data-downloadable-data)

## Related records

### Trials (209)

- A Combination Therapy Study of MK-2206 and AZD6244 in Participants With Advanced Solid Tumors (MK-2206-010)
- A Multi-centre Study to Assess the Safety, Tolerability, and Pharmacokinetics of Capivasertib (AZD5363) in Combination With Novel Agents in Patients With Metastatic Prostate Cancer
- A Phase 1b Study of T-DXd Combinations in HER2-low Advanced or Metastatic Breast Cancer
- A Phase I Study of MK-2206 in Combination With Standard Chemotherapy in Participants With Locally Advanced or Metastatic Solid Tumors (MK-2206-003)
- A Phase I Study to Investigate the Pharmacokinetics and Safety of Capivasertib in Participants With Moderate Hepatic Impairment
- A Phase I, Open-Label, First-Time-In-Human Study of the Oral AKT Inhibitor GSK2141795
- A Phase II Randomized Study Comparing the Efficacy and Safety of Targeted Therapy or Cancer Immunotherapy Versus Platinum-Based Chemotherapy in Patients With Cancer of Unknown Primary Site
- A Phase II Study of Akt Inhibitor MK2206 in the Treatment of Recurrent Platinum-Resistant Ovarian, Fallopian Tube, or Peritoneal Cancer
- A Phase IIIB Study to Evaluate the Use of Capivasertib in Combination With Fulvestrant in Patients With Advanced Breast Cancer Who Have Relapsed/Progressed on ET and CDK4/6 Inhibitor Reflecting Real World Clinical Practice in Spain
- A Rollover Study for Participants Previously Enrolled in a Genentech and/or F. Hoffman-La Roche Sponsored Study
- A Single-Arm Phase II Study of Neoadjuvant Intensified Androgen Deprivation (Leuprolide and Abiraterone Acetate) in Combination With AKT Inhibition (Capivasertib) for High-Risk Localized Prostate Cancer With PTEN Loss
- A Study Assessing the Safety and Efficacy of Adding Ipatasertib to Paclitaxel Treatment in Participants With Breast Cancer That Has Spread Beyond the Initial Site, and the Cancer Does Not Have Certain Hormonal Receptors
- A Study Conducted in Subjects With Relapsed/Refractory Multiple Myeloma (MM); to Determine Dose of Afuresertib in Combination With Carfilzomib (Part 1) and to Investigate the Safety, Pharmacokinetic and Clinical Activity of the Combination Compared With Carfilzomib Alone (Part 2)
- A Study Evaluating Targeted Therapies in Participants Who Have Advanced Solid Tumors With Genomic Alterations or Protein Expression Patterns Predictive of Response
- A Study Evaluating the Effect of Formulation on the Bioavailability of Ipatasertib in Healthy Volunteers
- A Study Evaluating the Efficacy and Safety of Biomarker-Driven Therapies in Patients With Persistent or Recurrent Rare Epithelial Ovarian Tumors
- A Study Evaluating the Efficacy and Safety of Multiple Treatment Combinations in Participants With Breast Cancer
- A Study Evaluating the Efficacy and Safety of Multiple Treatment Combinations in Patients With Metastatic or Locally Advanced Breast Cancer
- A Study Evaluating the Safety and Tolerability of GDC-0068 in Patients With Refractory Solid Tumors
- A Study Evaluating The Safety, Efficacy and Pharmacokinetics Of Ipatasertib In Combination With Atezolizumab And Docetaxel In Metastatic Castration-Resistant Prostate Cancer (mCRPC).

### Drugs (14)

- Afuresertib Serine/threonine-protein kinase AKT inhibitor
- [Capivasertib](https://trialight.com/data/asset/capivasertib-935ebe6a-a1c8-413b-8259-07e301a25a61.md) Serine/threonine-protein kinase AKT inhibitor
- GSK-690693 Serine/threonine-protein kinase AKT inhibitor
- Ipatasertib Serine/threonine-protein kinase AKT inhibitor
- LY-2780301 Serine/threonine-protein kinase AKT inhibitor
- Miransertib Serine/threonine-protein kinase AKT inhibitor
- MK-2201 Serine/threonine-protein kinase AKT inhibitor
- MK-2206 Serine/threonine-protein kinase AKT inhibitor
- Pifusertib Serine/threonine-protein kinase AKT negative allosteric modulator
- Rupitasertib Serine/threonine-protein kinase AKT3 inhibitor
- TAS0612 Serine/threonine-protein kinase AKT inhibitor
- Triciribine phosphate Serine/threonine-protein kinase AKT inhibitor
- Uprosertib Serine/threonine-protein kinase AKT inhibitor
- XL-418 Serine/threonine-protein kinase AKT inhibitor

---

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