Mutation within the Nmdar2 coding sequence; results in a premature stop codon.
An 8bp deletion starting in the fifth amino acid that causes a frameshift and early translation termination. There is also a 9bp deletion (TTGATCCTG - X:1502062..1502070:-1 ) beyond the early stop codon.
Nmdar2YH7/Nmdar2YH9 is a non-suppressor of abnormal neurophysiology | larval stage phenotype of Scer\GAL4VGlut1-OK371, VGlut1UAS.cDa
Nmdar2YH7 is a non-suppressor of abnormal neurophysiology | larval stage phenotype of Scer\GAL4VGlut1-OK371, VGlut1UAS.cDa
Nmdar2YH7/Nmdar2YH9 is a non-suppressor of embryonic/larval neuromuscular junction phenotype of Scer\GAL4VGlut1-OK371, VGlut1UAS.cDa
Nmdar2YH7 is a non-suppressor of embryonic/larval neuromuscular junction phenotype of Scer\GAL4VGlut1-OK371, VGlut1UAS.cDa
Nmdar2YH7 is a non-suppressor of muscle cell of A1-7 ventral longitudinal muscle 3 | larval stage phenotype of Scer\GAL4VGlut1-OK371, VGlut1UAS.cDa
Nmdar2YH7/Nmdar2YH9 is a non-suppressor of muscle cell of A1-7 ventral longitudinal muscle 3 | larval stage phenotype of Scer\GAL4VGlut1-OK371, VGlut1UAS.cDa