Gene:
ubiquitin fusion degradation 1-like
Gene ID:
128684
Symbol:
Ufd1l
Species:
1182
Description:
component of multiprotein complex; interacts with Npl4, involved in a degradation pathway for ubiquitin fused products; human homolog linked to the DiGeorge syndrome, a congenital developmental disorder with cardiac and craniofacial defects; deletion of mouse homolog is lethal [RGD]