Home > 分離済み変異体 > tm4856

分離済み変異体

Allele Name		tm4856
Balance		Not Required
OutCross		Not Accepted
Sequence Name		C17C3.18
Gene Name		ins-13
Worm Base	Allele Name	tm4856
	Gene Name	ins-13
	Sequence	C17C3.18
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)		14495/14496-14871/14872 (376 bp deletion)
Chromosome		II
Putative gene structure		complement(join(14476..14610, 14656..14742))
Map position		-1.17
Balancer
Map position of balancer
Sequence of primers		IntRev:CGGGTTAGCTCAAGGATGTT,ExtFwd:GATTGGCAGTGTAGTGGGTT,ExtRev:CTTCGCACATCCTGGACTGA,IntFwd:ACATGGATACCCAAGGGTTC
Distributed lab
Depositor		Dr. S. Mitani/NBRP
References		Please submit your publication Fernandes de Abreu DA, Caballero A, Fardel P, Stroustrup N, Chen Z, Lee K, Keyes WD, Nash ZM, López-Moyado IF, Vaggi F, Cornils A, Regenass M, Neagu A, Ostojic I, Liu C, Cho Y, Sifoglu D, Shen Y, Fontana W, Lu H, Csikasz-Nagy A, Murphy CT, Antebi A, Blanc E, Apfeld J, Zhang Y, Alcedo J, Ch'ng Q. An insulin-to-insulin regulatory network orchestrates phenotypic specificity in development and physiology. PLoS Genet 2014 10(3) e1004225  [ PubMed ID = 24675767 ] [ RRC reference ] Hung WL, Hwang C, Gao S, Liao EH, Chitturi J, Wang Y, Li H, Stigloher C, Bessereau JL, Zhen M. Attenuation of insulin signalling contributes to FSN-1-mediated regulation of synapse development. EMBO J 2013 32(12) 1745-60  [ PubMed ID = 23665919 ] [ RRC reference ]