| Primary Identifier | MGI:1918699 | Organism | mouse, laboratory |
| Chromosome | 1 | NCBI Gene Number | 71449 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0) Predicted to enable protein-lysine N-methyltransferase activity. Predicted to be involved in negative regulation of cell cycle G1/S phase transition and negative regulation of transcription by RNA polymerase II. Predicted to act upstream of or within methylation. Located in mitochondrion and nucleus. Is expressed in axial musculature and submandibular gland primordium. Orthologous to human METTL13 (methyltransferase 13, eEF1A N-terminus and K55). PHENOTYPE: Mice heterozygous for a null allele exhibit infertility, bilateral cryptorchism, abnormal spermatogenesis, and increased Leydig cell number. [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
