KEGG   VARIANT: 7874v1
Entry
7874v1                      Variant                                
Name
USP7 mutation
Type
Loss of function
Gene
USP7  ubiquitin specific peptidase 7 [KO:K11838]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 602519
Network
nt06523  Epigenetic regulation by Polycomb complexes
Disease
H02528  Hao-Fountain syndrome
Reference
  Authors
Fountain MD, Oleson DS, Rech ME, Segebrecht L, Hunter JV, McCarthy JM, Lupo PJ, Holtgrewe M, Moran R, Rosenfeld JA, Isidor B, Le Caignec C, Saenz MS, Pedersen RC, Morgan TM, Pfotenhauer JP, Xia F, Bi W, Kang SL, Patel A, Krantz ID, Raible SE, Smith W, Cristian I, Torti E, Juusola J, Millan F, Wentzensen IM, Person RE, Kury S, Bezieau S, Uguen K, Ferec C, Munnich A, van Haelst M, Lichtenbelt KD, van Gassen K, Hagelstrom T, Chawla A, Perry DL, Taft RJ, Jones M, Masser-Frye D, Dyment D, Venkateswaran S, Li C, Escobar LF, Horn D, Spillmann RC, Pena L, Wierzba J, Strom TM, Parenti I, Kaiser FJ, Ehmke N, Schaaf CP
  Title
Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies.
  Journal
Genet Med 21:1797-1807 (2019)
DOI:10.1038/s41436-019-0433-1
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