Fig. 3
From: A novel deletion mutation in KMT2A identified in a child with ID/DD and blood eosinophilia
Locations of ID/DD-associated KMT2A mutations. 22 mutations in affected individuals with ID/DD disorders are mapped. Colored boxes depict specific functional domains of the encoded protein using SMART program (http://smart.embl-heidelberg.de/). The mutation in red represents the current case. Four additional mutations with no predicted protein positions are not shown in the diagram