KEGG   VARIANT: 5295v1
Entry
5295v1                      Variant                                
Name
PIK3R1 mutation
Type
Loss of function
Gene
PIK3R1  phosphoinositide-3-kinase regulatory subunit 1 [KO:K02649]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 171833
Network
nt06537  TCR/BCR signaling
Disease
H00085  Agammaglobulinemias
H01370  SHORT syndrome
Reference
  Authors
Dyment DA, Smith AC, Alcantara D, Schwartzentruber JA, Basel-Vanagaite L, Curry CJ, Temple IK, Reardon W, Mansour S, Haq MR, Gilbert R, Lehmann OJ, Vanstone MR, Beaulieu CL, Majewski J, Bulman DE, O'Driscoll M, Boycott KM, Innes AM
  Title
Mutations in PIK3R1 cause SHORT syndrome.
  Journal
Am J Hum Genet 93:158-66 (2013)
DOI:10.1016/j.ajhg.2013.06.005
Reference
  Authors
Conley ME, Dobbs AK, Quintana AM, Bosompem A, Wang YD, Coustan-Smith E, Smith AM, Perez EE, Murray PJ
  Title
Agammaglobulinemia and absent B lineage cells in a patient lacking the p85alpha subunit of PI3K.
  Journal
J Exp Med 209:463-70 (2012)
DOI:10.1084/jem.20112533
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