Papers flagged by authors for seqchange
|WBPaper ID||Author comments
(checked means the author flagged the data type but left no additional comments)
|Date the data type was flagged|
|00035152||Allele - Location (Distance from start ATG in base pairs) - Mutation - Consequence
br1 - 1332 - a to t E268V
br12 - 965 - g to a - premature stop
br21 - 965 - g to a - premature stop
br22 - 1657 - g to a - aberrant splice junction
br29 - 1388 - a to t - H279L AND 1486 - g to a - G312E
br42 - 1284 - c to t - H245Y
ok2197 319â2060 deletion incomplete transcript
|00035166||ot81: 2281bp deletion from position 3282 to 5563 in the coordinates of fosmid K10C3||2009-09-21|
|00035158 (merged with 35179)||egl-9(ia58) is a 1bp deletion and causes a frameshift in exon 3. egl-9(ia60) is a MOS1 insertion in exon 3. egl-9(ia61) is a 5bp duplication and a nearby point mutation in exon 4.||2009-09-04|
|00035181||mak-2(ju637) change "CCGGAGAATTTAcTTTATGT" to "CCGGAGAATTTAtTTTATGT"
cebp-1(ju659) change "AAAATCGcGTAAAAA" to "AAAATCGtGTAAAAA"
cebp-1 (ju640) change "AAAATcGCGTAAAAA" to "AAAATtGCGTAAAAA"
|00035192||dhc-1(js319) is an AG -> AA mutation in the splice acceptor for exon 13.||2009-10-12|
|00035215||The nol-6(ac1) allele is a G to A substitution in the third exon of the C. elegans gene nol-6 resulting in a glycine to glutamic acid substitution at amino acid position 151||2009-10-01|
|00035247||lev-9(ox177): Mos1 insertion in the first exon between TA and TG 142 bases from the ATG.
lev-9(x62): TGG->TGA in the 6th exon 150 bases from the beginning of the 6th exon
lev-9(x16):TGG->TGA in the 11th exon 35 bases from the beginning of the 11th exon
|00035252||we sequenced and confirmed the available mitani deletion allele. moreover we generated a deletion allele for toca-2, named ng11, that appears to be a null allele by sequence analysis and by western blot.
ng11 (549-2333 (1784 bp deletion)) was generated using the random mutagenesis method with TMP/UV combined with gene-specific primer sets.
Back to Paper List