UASp regulatory sequences drive expression of csw containing the amino acid replacement A72S (this mutation is equivalent to the A72S mutation in the human ortholog Hsap\PTPN11, which is a mutation associated with Noonan syndrome in humans).
G2095281T
A72S | csw-PA; A125S | csw-PD
A72S
A72S mutation reported relative to isoform csw-PA; analogous mutation in human PTPN11 implicated in Noonan syndrome 1; mutation carried on in vitro construct; site of nucleotide substitution in fly gene and specific disease association inferred by FlyBase curator.
FlyBase curator comment: The mutation in cswA72S.Scer\UAS.P\T is associated with Noonan's syndrome in humans but although it results in various gain of function effects in transgenic flies it's not clear how these relate to the Noonan's syndrome phenotype.
Expression of cswA72S.Scer\UAS.P\T under the control of Scer\GAL4tub.PU results in lethality at the larval or pupal stage.
cswA72S.UASp/Scer\GAL4GMR.PU partially rescues cswlf
Expression of cswA72S.Scer\UAS.P\T under the control of Scer\GAL4GMR.PU partially rescues the rough eye phenotype of cswlf flies.