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Protein Coding Gene : Trmt10c tRNA methyltransferase 10C, mitochondrial RNase P subunit

Primary Identifier  MGI:1196261 Organism  mouse, laboratory
Chromosome  16 NCBI Gene Number  52575
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable identical protein binding activity and tRNA binding activity. Predicted to be involved in RNA processing and positive regulation of mitochondrial translation. Located in mitochondrion. Is expressed in several structures, including central nervous system; metanephros; phalanx; skin; and tooth. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 30. Orthologous to human TRMT10C (tRNA methyltransferase 10C, mitochondrial RNase P subunit).
  • synonyms:
  • RIKEN cDNA 1300018J16 gene,
  • tRNA methyltransferase 10C, mitochondrial RNase P subunit,
  • MGI:1922015,
  • Trmt10c,
  • RNA (guanine-9-) methyltransferase domain containing 1,
  • DNA segment, Chr 16, ERATO Doi 454, expressed,
  • D16Ertd454e,
  • 1300018J16Rik,
  • Rg9mtd1

Features --> Cross References

Genome

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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