Caution, this is an AI generated summary based on literature. This may have errors, see here for more.
Please share your feedback with us.
MT-TM: MT-TM is a mitochondrial gene that was found to be upregulated in a paediatric case, along with GDF15 and several other mitochondrial genes [PMC8803326]. This finding expands our understanding of the phenotypic spectrum of disease related to MT-TM mutations and the impact of pathogenic mt-tRNA gene variants in both paediatric and adult specialities [PMC6617384]. Additionally, CCL2 was found to be downregulated in the same case [PMC8803326]. This information suggests that MT-TM mutations may play a role in disease pathogenesis and highlights the importance of studying mitochondrial genes in various medical fields.
Genome locations
Gene Ontology annotations
Ancestor Chart
Loading ontology ancestors...
Failed to load QuickGO Ancestor chart
Sequence
Sequence features are shown above as colored rectangles.
Zoom in and click to view details, or
Reset