Homozygotes complete embryogenesis with no consistent cuticular phenotype, but never hatch.
SxlfP7B0, snRNP-U1-70K02107, snfJ210 has lethal phenotype
snRNP-U1-70K02107 has phenotype, suppressible by snRNP-U1-70K::Hsap\SRSF1Tag:FLAG
When mothers heterozygous for both snfJ210 and snRNP70K02107 are crossed with SxlfP7B0 males, a significant reduction in viability is seen in SxlfP7B0/+ daughters. When mothers heterozygous for both snfJ210 and snRNP70K02107 are crossed with SxlfP7B0 males, a significant reduction in viability is seen in SxlfP7B0/+ daughters.
The addition of snRNP70K::Hsap\SFRS1T:Zzzz\FLAG rescues the snRNP70K02107 phenotype.
snRNP-U1-70K02107 is rescued by snRNP-U1-70Khs.PS
snRNP-U1-70K02107 is rescued by snRNP-U1-70K+t9
A transgene construct lacking the arginine-rich domain also rescues the lethality.
A. Spradling.
Excision of the P-element restores viability, as do transgenes carrying either a wildtype genomic fragment or cDNA under the control of the Hsp70 promoter. Some partial revertants show partial female-specific lethality and defects in oogenesis.
"FBti0005210 == FBti0000289 == P{PZ}snRNP70K02107" was stated as revision.
Complements: Hrb27C02647. Complements: smt304493. Complements: smt304841. Complements: Hrb27C10280. Complements: smt310636. Complements: miltk06704. Complements: Coproxk10617. Complements: miltk14514b. Complements: cuc06491.