KEGG   VARIANT: 8905v1
Entry
8905v1                      Variant                                
Name
AP1S2 mutation
Type
Loss of function
Gene
AP1S2  AP-1 complex subunit sigma-2 isoform 2 [KO:K12394]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 300629
Network
nt06550  Lysosome biogenesis
Disease
H03038  Pettigrew syndrome
Reference
  Authors
Tarpey PS, Stevens C, Teague J, Edkins S, O'Meara S, Avis T, Barthorpe S, Buck G, Butler A, Cole J, Dicks E, Gray K, Halliday K, Harrison R, Hills K, Hinton J, Jones D, Menzies A, Mironenko T, Perry J, Raine K, Richardson D, Shepherd R, Small A, Tofts C, Varian J, West S, Widaa S, Yates A, Catford R, Butler J, Mallya U, Moon J, Luo Y, Dorkins H, Thompson D, Easton DF, Wooster R, Bobrow M, Carpenter N, Simensen RJ, Schwartz CE, Stevenson RE, Turner G, Partington M, Gecz J, Stratton MR, Futreal PA, Raymond FL
  Title
Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation.
  Journal
Am J Hum Genet 79:1119-24 (2006)
DOI:10.1086/510137
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