Skip to main content
Fig. 2 | BMC Genetics

Fig. 2

From: MECP2, a gene associated with Rett syndrome in humans, shows conserved coding regions, independent Alu insertions, and a novel transcript across primate evolution

Fig. 2

Comparison of human MECP2_e2 amino acid sequences with those from other primates. Top bar indicates different MECP2 regions with codon numbers delimiting each region. ID = interdomain. Numbers inside parentheses indicate the number of specimens analyzed. Ins* indicates an insertion between codons 357 and 358

Back to article page