KEGG   VARIANT: 2782v1
Entry
2782v1                      Variant                                
Name
GNB1 mutation
Type
Gain of function
Gene
GNB1  G protein subunit beta 1 [KO:K04536]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 139380
Network
nt06530  PI3K signaling
nt06544  Neuroactive ligand signaling
Disease
H00773  Autosomal dominant intellectual developmental disorder
Reference
  Authors
Petrovski S, Kury S, Myers CT, Anyane-Yeboa K, Cogne B, Bialer M, Xia F, Hemati P, Riviello J, Mehaffey M, Besnard T, Becraft E, Wadley A, Politi AR, Colombo S, Zhu X, Ren Z, Andrews I, Dudding-Byth T, Schneider AL, Wallace G, Rosen AB, Schelley S, Enns GM, Corre P, Dalton J, Mercier S, Latypova X, Schmitt S, Guzman E, Moore C, Bier L, Heinzen EL, Karachunski P, Shur N, Grebe T, Basinger A, Nguyen JM, Bezieau S, Wierenga K, Bernstein JA, Scheffer IE, Rosenfeld JA, Mefford HC, Isidor B, Goldstein DB
  Title
Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures.
  Journal
Am J Hum Genet 98:1001-10 (2016)
DOI:10.1016/j.ajhg.2016.03.011
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