Amino acid replacement: H844L.
Mutation in the second zinc finger of lola isoform T (PR/PG).
A10483085T
H389L | pre-lola-G-PC; H389L | pre-lola-G-PD; H844L | lola-PG; H844L | lola-PR
H844L
Reported relative to isoform K, which corresponds to FlyBase lola-PG and lola-PR. Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
gonad | embryonic stage (with lolae76)
lola46.38/lola22.05 and lola46.38/lolae76 transheterozygous embryos, but not lola46.38 heterozygotes, display a significant increase in defects in the fusion together and compaction of primordial germ cells and somatic gonadal precursor cells, as compared to controls.
lola46.38/lola22.05 transheterozygous embryos also display a significant increase in the number of extragonadal primordial germ cells, but no obvious defects in the development of the visceral mesoderm, as compared to controls.
lola46.38/lola22.05 has gonad | embryonic stage phenotype, enhanceable by rib55.25/rib[+]
lola46.38/lola22.05 has gonadal sheath proper primordium phenotype, enhanceable by rib55.25/rib[+]
lola46.38/lola22.05 has germline cell | embryonic stage phenotype, enhanceable by rib55.25/rib[+]
lola46.38, rib55.25/rib[+] has gonadal sheath proper primordium phenotype
lola46.38, rib55.25/rib[+] has gonad | embryonic stage phenotype
lola46.38, rib55.25/rib[+] has germline cell | embryonic stage phenotype
lola46.38/+, rib55.25/+ double heterozygous embryos display a very significant increase in defects in the fusion together and compaction of primordial germ cells and somatic gonadal precursor cells, as compared to controls.
The defects exhibited by lola46.38/lola22.05 transheterozygous embryos to fuse together and compact primordial germ cells and somatic gonadal precursor cells are significantly enhanced by heterozygosity for rib55.25.