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Details of TUFM gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| TUFM | --- | P49411 | EFTU_HUMAN | 7284
| ENSG00000178952
| Elongation factor Tu, mitochondrial | SPROT |
Disease |
|---|
| Disease |
OMIM id |
| Combined oxidative phosphorylation deficiency 4 (COXPD4) [MIM:610678]: A mitochondrial disease resulting in neonatal lactic acidosis, rapidly progressive encephalopathy, severely decreased mitochondrial protein synthesis, and combined deficiency of mtDNA- related mitochondrial respiratory chain complexes. Note=The disease is caused by mutations affecting the gene represented in this entry. |
610678 |
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
|
