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Protein Coding Gene : Mrm2 mitochondrial rRNA methyltransferase 2

Primary Identifier  MGI:1915267 Organism  mouse, laboratory
Chromosome  5 NCBI Gene Number  68017
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable rRNA (uridine-2'-O-)-methyltransferase activity. Predicted to be involved in RNA methylation and mitochondrial large ribosomal subunit assembly. Located in mitochondrion. Human ortholog(s) of this gene implicated in mitochondrial DNA depletion syndrome 17. Orthologous to human MRM2 (mitochondrial rRNA methyltransferase 2).
  • synonyms:
  • Mrm2,
  • Ftsj2,
  • RIKEN cDNA 2310037B18 gene,
  • mitochondrial rRNA methyltransferase 2,
  • FtsJ RNA methyltransferase homolog 2 (E. coli),
  • 2310037B18Rik,
  • FtsJ homolog 2 (E. coli)

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

0 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

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

Interactions

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

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0 Driver For