Table 3. Insertions with coincident or closely linked lethal mutations.
Original Symbol | Noncomplementing Deletions and Mutations | Phenotypea | New Insertion Symbol | New Allele Symbolsb | New Lethal Allele |
---|---|---|---|---|---|
Insertion and lethality may not be separable, but separate insertion and lethal locus named | |||||
P{lacW}l(2)SH0499SH0499 | Df(2R)BSC334, Df(2R)Exel7153 | v-l | P{lacW}MED9SH0499 | CG42518SH0499 | l(2)SH0499SH0499 |
P{lacW}l(2)45Aik00116 | Df(2R)BSC271 | l | P{lacW}CG8078k00116 | l(2)45Aik00116 | |
P{lacW}l(2)k02206k02206 | Df(2R)BSC402 | l | P{lacW}CG33785k02206 | CG33786k02206 | l(2)k02206k02206 |
P{lacW}l(2)k03201k03201 | Df(2L)BSC296, Df(2L)BSC354 | l | P{lacW}Sec61alphak03201 | l(2)k03201k03201 | |
P{lacW}l(2)k04003k04003 | Df(2L)ED623 | l | P{lacW}Trs23k04003 | l(2)k04003k04003 | |
P{lacW}l(2)k04308k04308 | Df(2R)BSC281, Df(2R)BSC303 | l | P{lacW}gemk04308 | l(2)k04308k04308 | |
P{lacW}l(2)k05448k05448 | Df(2L)BSC245, Df(2L)BSC290, Df(2L)Exel6034 | l | P{lacW}CG5776k05448 | l(2)k05448k05448 | |
P{lacW}l(2)k06204k06204 | Df(2R)BSC158, cl(2)k06205k06205 | l | P{lacW}Sec24ABk06204 | CR45467k06204 | l(2)k06204k06204 |
P{lacW}l(2)k06205k06205 | Df(2R)BSC158, cl(2)k06204k06204 | l | P{lacW}Sec24ABk06205 | CR45467k06205 | l(2)k06204k06205 |
P{lacW}l(2)k06502k06502 | Df(2L)ED270 | l | P{lacW}CG11030k06502 | l(2)k06502k06502 | |
P{lacW}l(2)k07215k07215 | Df(2L)BSC312, Df(2L)BSC302, Df(2L)Exel6047 | l | P{lacW}CG9246k07215 | l(2)k07215k07215 | |
P{lacW}l(2)k07408k07408 | Df(2R)BSC359 | l | P{lacW}AsnRS-mk07408 | l(2)k07408k07408 | |
P{lacW}l(2)k08601k08601 | Df(2R)X1 | l | P{lacW}Mef2k08601 | l(2)k08601k08601 | |
P{lacW}l(2)k09328k09328 | Df(2R)ED2308 | l | P{lacW}CG17574k09328 | l(2)k09328k09328 | |
P{lacW}l(2)k10105k10105 | Df(2L)BSC245 | l | P{lacW}CG5287k10105 | l(2)k10105k10105 | |
P{lacW}l(2)k10239k10239 | Df(2L)Exel7077 | l | P{lacW}sickk10239 | l(2)k10239k10239 | |
P{lacW}l(2)k10317k10317 | Df(2R)BSC360 | l | P{lacW}MESK2k10317 | l(2)k10317k10317 | |
P{lacW}l(2)k12402k12402 | Df(2R)BSC280 | l | P{lacW}prelk12402 | l(2)k12402k12402 | |
P{lacW}l(2)k13412k13412 | Df(2R)BSC279 | l | P{lacW}CG8026k13412 | CG45085k13412 | l(2)k13412k13412 |
P{lacW}l(2)k13604k13604 | Df(2L)ED21 | l | P{lacW}CG3645k13604 | l(2)k13604k13604 | |
P{lacW}l(2)k16204k16204 | Df(2R)Exel7164 | l | P{lacW}HnRNP-Kk16204 | l(2)k16204k16204 | |
P{lacW}l(2)k16805k16805 | Df(2R)BSC668 | l | P{lacW}Cpsf160k16805 | l(2)k16805k16805 | |
P{lacW}l(2)k17002k17002 | Df(2R)X58-12 | l | P{lacW}CG13510k17002 | CG13511k17002, CG42565k17002 | l(2)k17002k17002 |
P{PZ}l(2)0400804008 | Df(2L)Exel6028 | l | P{PZ}Ca-beta04008 | l(2)0400804008 | |
P{lacW}l(2)s4831s4831 | Df(2R)Exel7164 | l | P{lacW}HnRNP-Ks4831 | l(2)s4831s4831 | |
P{PZ}l(2)rG270rG270 | Df(2R)X58-12 | l | P{PZ}Vps20rG270 | l(2)rG270rG270 | |
P{PZ}l(2)0849208492 | Df(2R)Exel6054, Df(2R)Exel7092 | l | P{PZ}CG3049308492 | CG3049608492 | l(2)0849208492 |
P{PZ}l(2)1048110481 | Df(2R)Kr10, Df(2R)bwVDe2LPxKR | pl | P{PZ}lov10481 | l(2)1048110481 | |
Insertion and lethality may not be separable, but separate insertion and lethal locus already existed. | |||||
P{lacW}CG30007SH0071 | Df(2R)BSC158 | l | |||
P{lacW}CG8414SH0180 | Df(2R)ED2457 | l | |||
P{lacW}ZnT49BSH0360 | Df(2R)BSC485, Df(2R)Exel7121 | l | |||
P{lacW}CG6094SH0578 | Df(2L)BSC210, Df(2L)Exel7048 | l | |||
P{lacW}CG9641SH1104 | Df(2L)ED206 | l | |||
P{lacW}x16SH1297 | Df(2L)BSC108, Df(2L)ED6569 | l | |||
P{lacW}IntS8SH1314 | Df(2R)BSC382 | l | |||
P{lacW}clumsySH1386 | Df(2L)Exel6047 | l | |||
P{lacW}YL-1SH1685 | Df(2L)BSC145 | l | |||
Insertion not within the transcribed portion of a gene. Insertion and lethality may not be separable, but no separate lethal locus named. | |||||
P{lacW}l(2)k00302k00302 | Df(2L)BSC892 | l | |||
P{lacW}l(2)k07803k07803 | Df(2R)BSC298, Df(2R)B5 | l | |||
P{lacW}l(2)k09035k09035 | Df(2L)Exel6034 | l | |||
P{lacW}l(2)k11328k11328 | Df(2L)BSC277, Df(2L)BSC892, Df(2L)BSC290, Df(2L)ED784 | l | |||
P{lacW}l(2)k15817k15817 | Df(2L)BSC241 | l | |||
P{lacW}l(2)37Dbk16106 | Df(2L)Exel6042 | l | |||
P{PZ}l(2)0399603996 | Df(2R)BSC268 | l |
Phenotype in complementation tests: l, lethal; pl, partially lethal; v-l, homozygous viable but lethal in combination with deletions.
When an insertion lies in the region of gene overlap, FlyBase uses the symbol of one gene in the P insertion symbol and lists associated alleles for the other genes.
Original allele symbol.