Exosome component 3
Protein-coding gene in the species Homo sapiens
From Wikipedia, the free encyclopedia
Exosome component 3, also known as EXOSC3, is a human gene, which is part of the exosome complex.[5]
External IDsOMIM: 606489; MGI: 1913612; HomoloGene: 6867; GeneCards: EXOSC3; OMA:EXOSC3 - orthologs
Clinical significance
Mutations in EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration.[6]