KAT6B
Protein-coding gene in the species Homo sapiens
From Wikipedia, the free encyclopedia
K(lysine) acetyltransferase 6B (KAT6B) is an enzyme that in humans is encoded by the KAT6B gene.[5][6][7]
External IDsOMIM: 605880; MGI: 1858746; HomoloGene: 49310; GeneCards: KAT6B; OMA:KAT6B - orthologs
Interactions
Clinical significance
It has been demonstrated that de novo mutations in the gene KAT6B causes Young–Simpson syndrome and genitopatellar syndrome.[9][10][11][12][13]
