Gene

TRMT10C

Species
Homo sapiens
Symbol
TRMT10C
Name
tRNA methyltransferase 10C, mitochondrial RNase P subunit
Synonyms
  • COXPD30
  • FLJ20432
Biotype
protein coding gene
Automated Description
Enables identical protein binding activity; tRNA binding activity; and tRNA methyltransferase activity. Involved in RNA processing and positive regulation of mitochondrial translation. Located in mitochondrial nucleoid and nucleoplasm. Part of mitochondrial ribonuclease P complex and tRNA methyltransferase complex. Implicated in combined oxidative phosphorylation deficiency 30.
RGD Description
This gene encodes the precursor of a subunit of the mitochondrial ribonuclease P, which is involved in 5' processing of mitochondrial tRNAs. The encoded protein may confer RNA-binding capacity to mitochondrial ribonuclease P and may be essential for transcript processing, RNA modification, translation and mitochondrial respiration. [provided by RefSeq, Nov 2012]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR13563
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Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
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Annotation details
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    Disease Associations

    Cases where the expected disease association was NOT found
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    Alleles and Variants

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      Transgenic Alleles

      Species
      (carrying the transgene)
      Allele symbol
      Transgenic construct
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        Models

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          Sequence Feature Viewer

          Genome location
          Assembly version
          GRCh38
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          Sequence Details

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          Expression

          Primary Sources
          None
          Other Sources
          Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

          Molecular Interactions

          TRMT10C molecule type
          Interactor gene
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          Interactor molecule type
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            Genetic Interactions

            TRMT10C role
            TRMT10C genetic perturbation
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