Primary Identifier | MGI:2137600 | Organism | mouse, laboratory |
Chromosome | 5 | NCBI Gene Number | 94254 |
Mgi Type | protein coding gene |
description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Predicted to enable guanyl-nucleotide exchange factor activity and rRNA binding activity. Involved in mitochondrial fusion. Located in mitochondrial inner membrane. Human ortholog(s) of this gene implicated in Williams-Beuren syndrome. Orthologous to human RCC1L (RCC1 like). PHENOTYPE: Mice homozygous for a null allele exhibit early embryonic lethality. [provided by MGI curators] |