Insertion of a P{PZ} element within the 5' untranslated region, between positions 662 and 663 of intron 1.
follicle cell (with kst2)
kst01318/kst2 has follicle cell phenotype, non-enhanceable by sosief00514/CG13636[+]
kst01318/kst2 has follicle cell phenotype, non-suppressible by sosief00514/CG13636[+]
kst01318, vri5R7.2 has wing margin | posterior phenotype
kst01318, vri5R7.2 has wing margin | anterior phenotype
sosief00514/+ does not increase the penetrance of the follicle cell migration coordination defect (border cells migrating ahead of outer follicle cells) seen in kst2/kst01318 egg chambers.
A. Spradling.
Induced with: l(3)72Dq01318.
This allele was listed in the BDGP database as a lethal or sterile line during the period 1994-1999, but was discarded from the gene disruption project prior to the summary publication (FBrf0111489). Reasons for excluding lines from the collection described in FBrf0111489 include presence of more than one P insertion on the mutant chromosome, separation of lethality (or sterility) from the location of the insertion, and loss of lethality (or sterility) from the stock. Further information is available from http://www.fruitfly.org/bfd/ and from Dr. Spradling (spradling@mail1.ciwemb.edu).
Revertants fully complement kst1, kst2 and Df(3L)1226.
Complements: l(3)0914309143. Complements: l(3)neo91.
The lethality of the kst01318 chromosome is not associated with a closely linked P{PZ} insertion.