Amino acid replacement: G409S.
Nucleotide substitution: G1577A.
Point mutation.
G3147562A
G1577A
G409S | Mad-PA; G479S | Mad-PB
G409S
Mad10 heterozygotes exhibit wild-type levels of synaptic boutons.
Larval heterozygotes with Df(2L)JS17 exhibit reduced fat body, midgut defects and greatly reduced gastric caecae and dissected pupae exhibit absent or severely reduced imaginal discs.
Mad[+]/Mad10 is a suppressor of abnormal neuroanatomy | larval stage phenotype of Vps35EY14200
Mad[+]/Mad10 is a suppressor of visible phenotype of Scer\GAL4en-e16E, saxQ263D.UAS.cDa
ImpĪ²1170, Mad10 has abnormal neuroanatomy phenotype
Mad[+]/Mad10 is a suppressor of NMJ bouton phenotype of Vps35EY14200
Mad[+]/Mad10 is a suppressor of wing | posterior phenotype of Scer\GAL4en-e16E, saxQ263D.UAS.cDa
Mad[+]/Mad10 is a suppressor of wing vein | ectopic phenotype of Scer\GAL4en-e16E, saxQ263D.UAS.cDa
The increased bouton number at the neuromuscular junction that is seen in homozygous Vps35EY14200 larvae is suppressed by Mad10/+.
Df(1)su(s)R194/+ ; exNY1 Mad10 clones are recovered in adult eyes, although they are smaller than Df(1)su(s)R194/+ ; exNY1 clones.
Mad mutations can be placed in an allelic series based on relative severity of the maternal effect enhancement of weak dpp alleles: Mad1 < Mad7 < Mad12 < Mad10 < Mad5 < Mad3 < Mad2 < Mad11 < Mad6 < Mad4 < Mad8 < Mad9.