| Primary Identifier | MGI:1913419 | Organism | mouse, laboratory |
| Chromosome | 5 | NCBI Gene Number | 66169 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Predicted to be involved in positive regulation of protein targeting to mitochondrion; positive regulation of type 2 mitophagy; and regulation of protein stability. Located in mitochondrion. Orthologous to human TOMM7 (translocase of outer mitochondrial membrane 7). PHENOTYPE: Homozygous knockout affects cerebrovascular development and results in impaired post-natal growth and weight gain and death before weaning. [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
