Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 10102
MIM: 604723
HGNC: 12367
Ensembl: ENSG00000123297
Variants:
dbSNP: 10102
ClinVar: 10102
TCGA: ENSG00000123297
COSMIC: TSFM
RNA/Proteins
Expression (GTEx)
Pathways
| Pathway | Source | External ID |
|---|---|---|
| Organelle biogenesis and maintenance | REACTOME | R-HSA-1852241 |
| Mitochondrial translation | REACTOME | R-HSA-5368287 |
| Mitochondrial translation elongation | REACTOME | R-HSA-5389840 |
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38578353 | 2024 | Short-term regulation of TSFM level does not alter amyloidogenesis and mitochondrial function in type-specific cells. | 0 |
| 38578353 | 2024 | Short-term regulation of TSFM level does not alter amyloidogenesis and mitochondrial function in type-specific cells. | 0 |
| 27677415 | 2016 | Molecular-genetic characterization and rescue of a TSFM mutation causing childhood-onset ataxia and nonobstructive cardiomyopathy. | 13 |
| 27677415 | 2016 | Molecular-genetic characterization and rescue of a TSFM mutation causing childhood-onset ataxia and nonobstructive cardiomyopathy. | 13 |
| 25037205 | 2014 | Mitochondrial EFTs defects in juvenile-onset Leigh disease, ataxia, neuropathy, and optic atrophy. | 15 |
| 25037205 | 2014 | Mitochondrial EFTs defects in juvenile-onset Leigh disease, ataxia, neuropathy, and optic atrophy. | 15 |
| 21741925 | 2012 | Mutation in the mitochondrial translation elongation factor EFTs results in severe infantile liver failure. | 19 |
| 21741925 | 2012 | Mutation in the mitochondrial translation elongation factor EFTs results in severe infantile liver failure. | 19 |
| 20877624 | 2010 | Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression. | 20 |
| 20877624 | 2010 | Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression. | 20 |
| 17033963 | 2006 | Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTs. | 66 |
| 17033963 | 2006 | Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTs. | 66 |
Citation
Dessen P
TSFM (Ts translation elongation factor, mitochondrial)
Atlas Genet Cytogenet Oncol Haematol. 2014-08-01
Online version: http://atlasgeneticsoncology.org/gene/54728/tsfm-(ts-translation-elongation-factor-mitochondrial)
