| Gene Symbol | RHOT2 |
| Full Name | Ras Homolog Family Member T2 |
| Aliases | MIRO2, ARHI2, C16orf52 |
| Chromosome | 16p13.3. |
| Function | RHOT2 is a unique GTPase localized to the outer mitochondrial membrane that serves as a molecular hub connecting mitochondrial dynamics with cellular signaling. |
| Primary Expression | High in brain (substantia nigra), heart, skeletal muscle |
| Subcellular Localization | Mitochondrial outer membrane |
| Molecular Weight | ~68 kDa |
| Amino Acids | 618 aa |
| UniProt ID | Q8IXI2 |
| NCBI Gene ID | 55103 |
| Ensembl ID | ENSG00000150990 |
| OMIM | 612606 |
| GeneCards | RHOT2 |
| Human Protein Atlas | RHOT2 |
| Associated Diseases | neurodegeneration |
| Interactions | MIRO1 |
| KG Connections | 2 knowledge graph edges |
| Databases | GeneCardsHPASTRING |