Home > 分離済み変異体 > tm556

分離済み変異体

Allele Name		tm556
Balance		Not Required
OutCross		Not Accepted
Sequence Name		F37D6.2
Gene Name		row-1
Worm Base	Allele Name	tm556
	Gene Name	row-1
	Sequence	F37D6.2
Phenotype Information from the receiver is posted in the form of a "researcher : phenotype"		homozygous viable. Dr. M. Bastiani: no axon regeneration phenotype.
Mutation site Please see gene structure to locate the deletion in relation to exon(s)		1749/1750-2242/2243 (493 bp deletion)
Chromosome		I
Putative gene structure		complement(join(8..89,138..232,276..383,584..1064, 1114..1253, 1301..1505, 1551..1672, 1721..1913, 2057..2299, 2351..2430))
Map position		5.05
Balancer
Map position of balancer
Sequence of primers		ExtRev:CATTCCACCCTCACTCCCCT,ExtFwd:TAGACCGACGACATTTGTGA,IntRev:CCCCTGATCAACGGATCGAT,IntFwd:GTTCGGTTCCCATTCCACGA
Distributed lab
Depositor		Dr. S. Mitani
References		Please submit your publication McDiarmid TA, Belmadani M, Liang J, Meili F, Mathews EA, Mullen GP, Hendi A, Wong WR, Rand JB, Mizumoto K, Haas K, Pavlidis P, Rankin CH. Systematic phenomics analysis of autism-associated genes reveals parallel networks underlying reversible impairments in habituation. Proc Natl Acad Sci U S A 2020 117(1) 656-667  [ PubMed ID = 31754030 ] [ RRC reference ] Nix P, Hammarlund M, Hauth L, Lachnit M, Jorgensen EM, Bastiani M. Axon regeneration genes identified by RNAi screening in C. elegans. J Neurosci 2014 34(2) 629-45  [ PubMed ID = 24403161 ] [ RRC reference ]