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. Author manuscript; available in PMC: 2013 Sep 4.
Published in final edited form as: Autoimmunity. 2013 Jan 17;46(2):83–101. doi: 10.3109/08916934.2012.749244

Figure 2.

Figure 2

AID functional domains and functional altering mutations. The bottom panel showing the naturally occurring mutations in the AID gene that are responsible for the autosomal recessive disorder hyper-IgM syndrome type 2 (HIGM2). These mutations, as well as experimentally generated mutations in the AID gene, cause defects in CSR and/or SHM.