Chromosome 6q24-Q25 Deletion Syndrome

Chromosome 6q24-Q25 Deletion Syndrome, also known as 6q25 microdeletion syndrome, is related to coffin-siris syndrome 1 and microcephaly. An important gene associated with Chromosome 6q24-Q25 Deletion Syndrome is DEL6Q24Q25 (Chromosome 6q25-Q25 Deletion Syndrome), and among its related pathways/superpathways are 22q11.2 copy number variation syndrome and RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known. Affiliated tissues include eye and bone, and related phenotypes are global developmental delay and microcephaly