| Primary Identifier | MGI:1914917 | Organism | mouse, laboratory |
| Chromosome | 9 | NCBI Gene Number | 67667 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Enables iron ion binding activity and tRNA (5-carboxymethyluridine(34)-5-O)-methyltransferase activity. Involved in tRNA methylation and tRNA wobble uridine modification. Predicted to be located in cytosol and nucleoplasm. Predicted to be active in cytoplasm and nucleus. Is expressed in several structures, including blastocyst; early embryo; nervous system; secondary oocyte; and sensory organ. Human ortholog(s) of this gene implicated in autosomal recessive intellectual developmental disorder 71. Orthologous to human ALKBH8 (alkB homolog 8, tRNA methyltransferase). PHENOTYPE: Homozygous mutants show no obvious phenotype at 20 months of age. [provided by MGI curators] |
Features --> Cross References
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
