Amino acid replacement: V509D.
T9596698A
V560D | clos-PD
V509D
The site of the amino acid substitution was reported relative to an earlier version of the clos gene annotation which lacked the current 55aa starting exon and had an additional four amino acids in the next exon (previously the starting exon). Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Females containing homozygous germline clones give rise to embryos with a terminal phenotype; anterior and posterior terminal structures do not form.
Anterior and posterior terminal structures do not form in embryos derived from clos1/Df(2R)BSC132 females.
87% of eggs derived from clos1/Df(2R)BSC132 females show permeability to the neutral red dye, indicating a defect in vitelline membrane integrity.
clos1 has embryo | terminal expression pattern phenotype, suppressible by toract.RL3
The loss of anterior and posterior terminal structures seen in embryos derived from females containing homozygous clos1 germline clones is completely rescued by toract.RL3.
Df(2R)BSC132/clos1 is rescued by clos+t15.8
The loss of anterior and posterior terminal structures seen in embryos derived from clos1/Df(2R)BSC132 females is completely rescued by clos+t15.8.