分離済み変異体

tm6983

Allele Nametm6983
BalanceNot Required
OutCrossNot Accepted
Sequence NameF18A11.5
Gene NameF18A11.5
Worm BaseAllele Name tm6983
Gene Name F18A11.5
Sequence F18A11.5
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) 61899/61900-62466/62467 (567 bp deletion)
ChromosomeII
Putative gene structure[Y38F1A] complement(join(59689..60143, 61431..61503, 61615..61753, 61860..62017, 62071..62235, 63152..63262, 63309..63329))
Map position13.53
Balancer
Map position of balancer
Sequence of primersIntRev:GGCCGTTTGTCGAAAGAGGA,ExtRev:AAACGGTCGATTGCACCATG,IntFwd:GTTGACCATTGTCCCAGGCA,ExtFwd:CAGCATTCCTGGAACCTTAC
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 ]