| Primary Identifier | MGI:3790484 | Organism | mouse, laboratory |
| Chromosome | 14 | Mgi Type | complex/cluster/region |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 9.1.0) Used to study Feingold syndrome. PHENOTYPE: Homozygous deletion of this Mirn cluster results in neonatal lethality. Lung hypoplasia is observed in late gestation and newborn mice; fetal and adult B cell development are compromised also. [provided by MGI curators] |