Home > 分離済み変異体 > tm11669

分離済み変異体

Allele Name		tm11669
Balance		Not Required
OutCross		Completed
Sequence Name		F52D10.3
Gene Name		ftt-2
Worm Base	Allele Name	tm11669 (x1)
	Gene Name	ftt-2
	Sequence	F52D10.3
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)		21945/21946-22215/22216 (270 bp deletion)
Chromosome		X
Putative gene structure		complement(join(21082..21240, 21498..21661, 21937..22309, 22359..22409))
Map position		4.89
Balancer		tmC24[tmIs1240 tm9719]
Map position of balancer
Sequence of primers		ExtFwd:TCAAGTGCCTCCGCGTAAGC,ExtRev:TTCTACAAGGGCTCATACGC
Distributed lab
Depositor		Dr. 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 ]