分離済み変異体

tm5779

Allele Nametm5779
BalanceNot Required
OutCrossNot Accepted
Sequence NameF23H11.4
Gene NameF23H11.4
Worm BaseAllele Name tm5779
Gene Name F23H11.4
Sequence F23H11.4
Phenotype Information from the receiver is posted in the form of a "researcher : phenotype" homozygous viable.
Mutation site Please see gene structure to locate the deletion in relation to exon(s) 10692/10693-GACATTTT-11506/11507 (814 bp deletion + 8 bp insertion)
ChromosomeIII
Putative gene structurecomplement(join(6667..6927, 7031..7423, 8010..8075, 8147..8427, 8500..8634, 8885..8999, 9043..9169, 9850..10448, 10502..11028, 11171..11355, 11404..11687, 11735..11773))
Map position-25.36
Balancer
Map position of balancer
Sequence of primersIntRev:CCTATCAGATTCGCCCATAG,IntFwd:GTATGGAGTATCGGAAGCCA,ExtRev:TACCCTAGGTCTAAGCTTAG,ExtFwd:CGGAGGATCTTCTGGGATAA
Distributed lab
DepositorDr. S. Mitani/NBRP
References Please submit your publication
Mazzetto M, Gonzalez LE, Sanchez N, Reinke V.
Characterization of the distribution and dynamics of chromatin states in the C. elegans germline reveals substantial H3K4me3 remodeling during oogenesis.
Genome Res 2024 34(1) 57-69 
[ PubMed ID = 38164610 ] [ RRC reference ]