By reviewing previous literature in the Human Gene Mutation Database (HGMD), we found out thirty-two different ANXA11 variants have been identified in ALS and/or ALS–FTD, including patients from the United Kingdom, Southern Africans, Brazil, France, German, Korea, Spain, Japan, and China (Table 2) (14–26). Here, ANXA11 is linked to amyotrophic lateral sclerosis.