MTG1
mitochondrial ribosome associated GTPase 1
Summary
Enables GTPase activity. Involved in mitochondrial large ribosomal subunit assembly; regulation of mitochondrial translation; and regulation of respiratory system process. Located in mitochondrial inner membrane; mitochondrial ribosome; and nucleoplasm. Is active in mitochondrial matrix. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs530832129 | 10:135,207,732 | T/C | — | uncertain significance |
| rs1283218633 | 10:135,207,738 | C/T | — | uncertain significance |
| rs370553422 | 10:135,207,740 | C/T | — | uncertain significance |
| rs374714619 | 10:135,207,754 | C/G | — | likely benign |
| rs2493916558 | 10:135,207,763 | G/C | — | uncertain significance |
| rs1849745980 | 10:135,207,783 | T/G | — | uncertain significance |
| rs962645352 | 10:135,209,229 | T/C | — | uncertain significance |
| rs147793884 | 10:135,209,241 | T/A | — | uncertain significance |
| rs766433899 | 10:135,209,249 | G/C | — | uncertain significance |
| rs2493921459 | 10:135,209,676 | T/G | — | uncertain significance |
| rs147934877 | 10:135,209,680 | G/C | — | uncertain significance |
| rs762808360 | 10:135,209,698 | A/G | — | uncertain significance |
| rs370302182 | 10:135,213,045 | T/C | — | uncertain significance |
| rs1664213380 | 10:135,213,072 | G/A | — | uncertain significance |
| rs200334430 | 10:135,215,075 | C/A | — | uncertain significance |
| rs144012069 | 10:135,215,667 | C/T | — | benign |
| rs765788482 | 10:135,215,668 | C/A | — | uncertain significance |
| rs369817660 | 10:135,215,671 | A/G | — | uncertain significance |
| rs1300055867 | 10:135,215,729 | G/A | — | uncertain significance |
| rs2493935350 | 10:135,216,222 | G/A | — | uncertain significance |
| rs773693409 | 10:135,216,231 | A/G | — | uncertain significance |
| rs766023797 | 10:135,216,239 | C/G | — | uncertain significance |
| rs985894314 | 10:135,216,241 | A/G | — | uncertain significance |
| rs1197397951 | 10:135,216,252 | A/C | — | uncertain significance |
| rs746818212 | 10:135,216,270 | C/T | — | uncertain significance |
| rs2265908 | 10:135,217,956 | G/T | — | — |
| rs10857712 | 10:135,225,666 | T/C | regulatory region variant | — |
| rs747561455 | 10:135,232,988 | G/A | — | uncertain significance |
| rs140544603 | 10:135,233,032 | C/T | — | likely benign |
| rs768253637 | 10:135,233,067 | C/T | — | uncertain significance |
| rs971162539 | 10:135,233,575 | A/C | — | uncertain significance |
| rs11553728 | 10:135,233,628 | G/A | — | uncertain significance |
| rs762012935 | 10:135,233,637 | C/T | — | uncertain significance |
| rs201924847 | 10:135,233,650 | C/T | — | uncertain significance |
| rs1850208870 | 10:135,233,658 | A/C | — | uncertain significance |
| rs150570239 | 10:135,233,664 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.