Figure 2 | Genetics in Medicine

Figure 2

From: Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity

Figure 2

Overview of the aberrations involving chromosome band 2p25.3 from this study, patients from the literature,2,11,12,14,15,16 and two additional patients from the DatabasE of Chromosomal Imbalance and Phenotype in Humans using Ensembl Resources, pinpointing MYT1L as the only commonly disrupted gene. Red bars display deletions and blue bars represent duplications. The de novo splice-site mutations (patients 14 and 15) are depicted as short, vertical black lines. The RefSeq genes are gray. Genomic positions are according to GRCh37.

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