1 => The disorder is placed on the map based on its association with a gene, but the underlying defect is not known
2 => The disorder has been placed on the map by linkage; no mutation has been found
3 => The molecular basis for the disorder is known; a mutation has been found in the gene
4 => A contiguous gene deletion or duplication syndrome, multiple genes are deleted or duplicated causing the phenotype
| Gene Symbol | Chromosomal Location | Gene MIM number | Mapping Method | Phenotype | Phenotype MIM number | Phenotype Mapping Key |
| AKT1 | 14q32.33 | 164730 | REa, A | Breast cancer, somatic, 114480 (3) | 114480 | 3 |
| AKT1 | 14q32.33 | 164730 | REa, A | Colorectal cancer, somatic, 114500 (3) | 114500 | 3 |
| AKT1 | 14q32.33 | 164730 | REa, A | Ovarian cancer, somatic, 167000 (3) | 167000 | 3 |
| AKT1 | 14q32.33 | 164730 | REa, A | {Schizophrenia, susceptibility to}, 181500 (2) | 181500 | 2 |
| AKT1 | 14q32.33 | 164730 | REa, A | Proteus syndrome, somatic, 176920 (3) | 176920 | 3 |
| AKT1 | 14q32.33 | 164730 | REa, A | Cowden syndrome 6, 615109 (3) | 615109 | 3 |