Heterozygotes show a direct effect on the shape of the wing.
tkv8/tkvk16713 has abnormal neuroanatomy | third instar larval stage phenotype, non-suppressible by Ube3a35/Ube3a35
tkv8/tkvk16713 is a suppressor of abnormal neuroanatomy | third instar larval stage phenotype of Ube3a35
tkvk16713/tkv[+] is a suppressor of abnormal neuroanatomy | third instar larval stage phenotype of Rab81/Rab8B229
tkvk16713/tkv7 is a suppressor of abnormal neuroanatomy | third instar larval stage phenotype of Rab81/Rab8B229
tkvk16713/tkv7 is a suppressor of abnormal neuroanatomy phenotype of spictmut
tkvk16713 is a suppressor of visible phenotype of upd1GMR.PB
tkvk16713/tkv7 is a suppressor of abnormal neuroanatomy phenotype of spink09905/spin10403
tkv8/tkvk16713 has NMJ bouton | third instar larval stage phenotype, non-suppressible by Ube3a35/Ube3a35
tkv8/tkvk16713 is a suppressor of NMJ bouton | increased number | third instar larval stage phenotype of Ube3a35
tkvk16713/tkv[+] is a suppressor of embryonic/larval neuromuscular junction | third instar larval stage phenotype of Rab81/Rab8B229
tkvk16713/tkv[+] is a suppressor of NMJ bouton | third instar larval stage phenotype of Rab81/Rab8B229
tkvk16713/tkv7 is a suppressor of embryonic/larval neuromuscular junction | third instar larval stage phenotype of Rab81/Rab8B229
tkvk16713/tkv7 is a suppressor of NMJ bouton | third instar larval stage phenotype of Rab81/Rab8B229
tkvk16713/tkv7 is a suppressor of embryonic/larval neuromuscular junction phenotype of spictmut
tkvk16713 is a suppressor of eye phenotype of upd1GMR.PB
tkvk16713/tkv7 is a suppressor of bouton | increased number phenotype of spink09905/spin10403
tkvk16713/tkv7 is a suppressor of neuromuscular junction phenotype of spink09905/spin10403
DysE6, tkvk16713/tkv[+] has posterior crossvein phenotype
spin10403/spink09905 animals which are also mutant for tkv7/tkvk16713 show a decrease in bouton number.
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).
Complements: cype03771. Complements: l(2)k01302k01302. Complements: vrik05901.