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TRMT10C;jsessionid=683F6B510B3EECE35D6B9FE1F8161A98
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Jejunum
Peritoneum
Skeletal muscle
Prefrontal cortex
Tongue main corpus
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Disease Atlas
Most Correlated Diseases
Rift valley fever
Metabolic syndrome X
Placental insufficiency
Infection due to Propionibacterium
Chronic fatigue syndrome
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Most Correlated Compounds
Imidazoles
10058-F4 compound
Soman
pyroxamide
HI 6
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Most Correlated Gene Perturbations
Ar
SALL4
USP18
Mir155
TNFRSF1A
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Literature
Most Relevant Literature
The MRPP1/MRPP2 complex is a tRNA-maturation platform in human mitochondria.
Mutation or knock-down of 17β-hydroxysteroid dehydrogenase type 10 cause loss of MRPP1 and impaired …
Reduction of Drosophila Mitochondrial RNase P in Skeletal and Heart Muscle Causes Muscle Degeneratio…
Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respirator…
Disease-associated mutations in mitochondrial precursor tRNAs affect binding, m1R9 methylation, and …
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There were no clinical trials for TRMT10C;jsessionid=683F6B510B3EECE35D6B9FE1F8161A98
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