Amino acid replacement: C629Y. Residue resides in the transmembrane domain I-S1 closer to the extracellularside.
G16173759A
C136Y | Ca-alpha1D-PF; C136Y | Ca-alpha1D-PG; C136Y | Ca-alpha1D-PH; C136Y | Ca-alpha1D-PI; C136Y | Ca-alpha1D-PJ; C782Y | Ca-alpha1D-PK; C782Y | Ca-alpha1D-PL; C782Y | Ca-alpha1D-PM; C782Y | Ca-alpha1D-PN; C814Y | Ca-alpha1D-PO
Ca-α1DAR66 third instar larvae exhibit decreased locomotion.
Ca-α1DAR66 larvae exhibit a decrease in neuropeptide (Dilp2-GFP) release in type I boutons (on muscle 4) upon activation of RP2 motor neuron via exposure to high potassium.
In uncrowded conditions 48% eclose as adults although development is delayed by 1-2 days. Wings are usually unexpanded and many flies are found stuck in the food. The remaining 52% have difficulty eclosing and die as pharate adults. Transheterozygotes with Ca-α1DX7 are almost all able to escape the puparium but few transheterozygotes with Ca-α1DX10 succeed. A few homozygotes exhibit neurons in the longitudinal tracts that appear to stall at some of the commissures, forming nodular growths. Motoneurons in the SNb branch of the developing PNS also show stalling at stage 17. The defects may be due to a second lesion on the chromosome or generated by altered channel properties caused by the missense mutation.
Two-electrode voltage clamping of the larval body wall muscles demonstrates the total current is reduced in homozygotes, current is intermediate with wild type in heterozygotes. Total current is comprised of the A- and D-current, the D-current is significantly reduced by application of amiloride or inactivation of the A-current, A-currents remain unaffected. Mutant also exhibits a slowing of channel activation kinetics.
Ca-α1DAR66 is a suppressor of abnormal neuroanatomy phenotype of sei2
Ca-α1DAR66 is a suppressor of abnormal neuroanatomy phenotype of slo98
Ca-α1DAR66 is a suppressor of abnormal neuroanatomy phenotype of slo1
Ca-α1DAR66/Ca-alpha1D[+] is a non-suppressor of lethal phenotype of Cam7/Camn339
Ca-α1DAR66 is a suppressor of neuromuscular junction phenotype of slo1
Ca-α1DAR66 is a suppressor of NMJ bouton | increased number phenotype of sei2
Ca-α1DAR66 is a suppressor of neuromuscular junction phenotype of sei2
Ca-α1DAR66 is a suppressor of NMJ bouton | increased number phenotype of slo98
Ca-α1DAR66 is a suppressor of neuromuscular junction phenotype of slo98
Ca-α1DAR66 is a suppressor of NMJ bouton | increased number phenotype of slo1
Ca-α1DAR66/Ca-alpha1D[+] is a suppressor | partially of pupa phenotype of Cam7/Camn339
A Ca-α1DAR66 mutant background suppresses both type B and type M satellites in Ca-α1DAR66; slo1 or Ca-α1DAR66; slo98 double mutants nearly to wild-type levels. Such suppression in satellite formation leads to the morphology of these double mutants to resemble Ca-α1DAR66 single mutants.
A Ca-α1DAR66 mutant background suppresses both type B and type M satellites in Ca-α1DAR66; sei2 double mutants nearly to wild-type levels. Such suppression in satellite formation leads to the morphology of these double mutants to resemble Ca-α1DAR66 single mutants.
Ca-α1DAR66/+ has a slight suppressing effect on the Cam7/Camn339 phenotype; there is an increase in the pupal length:width ratio, but none of the pupae eclose.
Ca-α1DAR66 is rescued by Ca-α1D+tCa01
S. Roth.