Previous symbols: MTTF. Aliases: trnF.
Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.
| Disorder | Relationship | Where the gene appears |
|---|---|---|
| MERRF Syndrome | causative | |
| MTO1 Deficiency | modifier |
An entry matches when ClinGen's MONDO disease is the entry's own disease term, a subtype term, or an exact-match mapping. An amber status marks an entry ClinGen supports the gene for (Definitive, Strong or Moderate) whose own record does not type it. A Limited, Disputed or Refuted tier on such an entry is not a gap.
| ClinGen disease | MOI | Classification | dismech entry |
|---|---|---|---|
| familial juvenile hyperuricemic nephropathy MONDO:0000608 | MT | Moderate 2024-02-12 |
no dismech entry |
| mitochondrial disease MONDO:0044970 | MT | Definitive 2023-02-16 |
no dismech entry |
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.