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分離済み変異体

Allele Name		tm819
Balance		Completed
OutCross		Not Accepted
Sequence Name		C52E12.2
Gene Name		unc-104
Worm Base	Allele Name	tm819 (x1)
	Gene Name	unc-104
	Sequence	C52E12.2
Phenotype Information from the receiver is posted in the form of a "researcher : phenotype"		Lethal or sterile. Dr. E. Jorgensen: subviable on OP50 but can be manintained on HB101. Dr. Z. Zhou: no persistent cell corpses.
Mutation site Please see gene structure to locate the deletion in relation to exon(s)		9466/9467-CGATAGAGC-10725/10726 (1259 bp deletion + 9 bp insertion)
Chromosome		II
Putative gene structure		join(2872..2971, 3496..3646, 3694..3862, 3913..4091, 8659..8914, 9243..9403, 9452..9904, 10332..10600, 10648..10802, 10850..10970, 11241..11439, 11597..11728, 13408..13630, 13781..13916, 13964..14084, 14132..14279, 14326..14486, 14707..15340, 15562..15849, 16090..16222, 16269..16713, 17027..17147)
Map position		0.21
Balancer		,mIn1 [e128 mIs14]
Map position of balancer
Sequence of primers		IntRev:CGTCAACATTCGTTCTCCTT,ExtRev:CGCCGCCTTTCAAAAAAAGA,IntFwd:CTACAGGAGCGGAAGGTCAA,ExtFwd:AGGATCCGAAAGAGCCAATT
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 ] Anazawa Y, Kita T, Iguchi R, Hayashi K, Niwa S. De novo mutations in KIF1A-associated neuronal disorder (KAND) dominant-negatively inhibit motor activity and axonal transport of synaptic vesicle precursors. Proc Natl Acad Sci U S A 2022 119(32) e2113795119  [ PubMed ID = 35917346 ] [ RRC reference ]