- methionyl-tRNA
formyltransferase is a
protein that in
humans is
encoded by the
MTFMT gene. The
protein encoded by this
nuclear gene
localizes to the mitochondrion...
- methionyl-tRNA
formyltransferase (
MTFMT) in
patients with
Leigh syndrome. The c.626C>T
mutation identified in
MTFMT yielding symptoms of
Leigh Syndrome...
- HGNC:28785 Q7Z6M4 9978 MTF1 HGNC:7428 Q14872 9979 MTF2 HGNC:29535 Q9Y483 9980
MTFMT HGNC:29666 Q96DP5 9981 MTFP1 HGNC:26945 Q9UDX5 9982 MTFR1 HGNC:29510 Q15390...
- NDUFV1, NDUFS8, NDUFC2, TMEM126B, FOXRED1, NDUFA9, NDUFA12, NUBPL, NDUFAF1,
MTFMT, NDUFB10, NDUFAF8, NDUFV2, NDUFS7, NDUFA11, NDUFB7, NDUFA13, NDUFAF5, NDUFA6...
- NDUFA2, NDUFA11, NDUFAF3, NDUFAF10, NDUFB3, NDUFB9, ACAD9, FOXRED1, and
MTFMT. NDUFS4 has been
shown to have 58
binary protein-protein
interactions including...
- Patel, J., Goldberger, O. A., ... & Mootha, V. K. (2011).
Mutations in
MTFMT underlie a
human disorder of
formylation causing impaired mitochondrial...
