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Literature summary for 2.1.1.61 extracted from

  • Yan, Q.; Bykhovskaya, Y.; Li, R.; Mengesha, E.; Shohat, M.; Estivill, X.; Fischel-Ghodsian, N.; Guan, M.X.
    Human TRMU encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase is a putative nuclear modifier gene for the phenotypic expression of the deafness-associated 12S rRNA mutations (2006), Biochem. Biophys. Res. Commun., 342, 1130-1136.
    View publication on PubMed

Application

Application Comment Organism
additional information putative nuclear modifier gene TRMU may modulate the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA mutations Homo sapiens

Cloned(Commentary)

Cloned (Comment) Organism
TRMU-GFP fusion protein transfected into 143B cell line Homo sapiens

Localization

Localization Comment Organism GeneOntology No. Textmining
mitochondrion localizes exclusively to mitochondria, even when overexpressed Homo sapiens 5739
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Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
47750
-
sequence analysis Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens O75648
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Source Tissue

Source Tissue Comment Organism Textmining
brain moderately expressed Homo sapiens
-
colon low level Homo sapiens
-
heart abundantly expressed in tissues with high metabolic rates Homo sapiens
-
kidney abundantly expressed in tissues with high metabolic rates Homo sapiens
-
leukocyte low level Homo sapiens
-
liver low level Homo sapiens
-
lung low level Homo sapiens
-
placenta moderately expressed Homo sapiens
-
skeletal muscle abundantly expressed in tissues with high metabolic rates Homo sapiens
-
small intestine moderately expressed Homo sapiens
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spleen moderately expressed Homo sapiens
-
thymus low level Homo sapiens
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Synonyms

Synonyms Comment Organism
5-methylaminomethyl-2-thiouridylate-methyltransferase
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Homo sapiens
TRMU
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Homo sapiens