Primary Identifier | MGI:1920025 | Organism | mouse, laboratory |
Chromosome | 17 | NCBI Gene Number | 72775 |
Mgi Type | protein coding gene |
description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Predicted to be located in centrosome; chromosome; and nucleoplasm. Predicted to be part of Fanconi anaemia nuclear complex and chromatin. Is expressed in central nervous system; liver; metanephros; and retina. Human ortholog(s) of this gene implicated in Fanconi anemia complementation group E. Orthologous to human FANCE (FA complementation group E). PHENOTYPE: Homozygous knockout causes reduced male fertility. [provided by MGI curators] |