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分離済み変異体

Allele Name		tm6057
Balance		Not Required
OutCross		Not Accepted
Sequence Name		F10C2.5
Gene Name		F10C2.5
Worm Base	Allele Name	tm6057
	Gene Name	F10C2.5
	Sequence	F10C2.5
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)		23129/23130-23950/23951 (821 bp deletion)
Chromosome		V
Putative gene structure		join(22719..23151, 23205..23399, 23448..24040, 24103..24417, 24464..24991, 25436..25717)
Map position		3.61
Balancer
Map position of balancer
Sequence of primers		ExtFwd:GGCAAGTGCCGTCATCGAAC,IntFwd:CCAGGCACCTACTAAATGAA,IntRev:CATCCTTTGTCGCTCTATAC,ExtRev:GCCACATTTAGTTCGGGCTG
Distributed lab
Depositor		Dr. S. Mitani/NBRP
References		Please submit your publication Jablonski AM, Lamitina T, Liachko NF, Sabatella M, Lu J, Zhang L, Ostrow LW, Gupta P, Wu CY, Doshi S, Mojsilovic-Petrovic J, Lans H, Wang J, Kraemer B, Kalb RG. Loss of RAD-23 Protects Against Models of Motor Neuron Disease by Enhancing Mutant Protein Clearance. J Neurosci 2015 35(42) 14286-306  [ PubMed ID = 26490867 ] [ RRC reference ]