分離済み変異体

tm2661

Allele Nametm2661
BalanceNot Required
OutCrossNot Accepted
Sequence NameD1014.8
Gene Namespr-1
Worm BaseAllele Name tm2661
Gene Name spr-1
Sequence D1014.8
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) 10193/10194-10874/10875 (681 bp deletion)
ChromosomeV
Putative gene structurecomplement(join(8683..8760, 8815..8924, 8971..9197, 9251..9404, 9450..9560, 9610..9742, 10080..10274, 10330..10491, 10542..10756, 10799..10889, 10941..11141))
Map position1.02
Balancer
Map position of balancer
Sequence of primersExtFwd:CTGGACGATTCATCGCGTTA,ExtRev:ATAGCAGGTCCCGAAACTGA,IntFwd:CCCCGGTGCAATAGACAAAT,IntRev:GTGGATTCTCCACGCCCATC
Distributed lab
DepositorDr. S. Mitani
References Please submit your publication
Robinson SB, Refai O, Hardaway JA, Sturgeon S, Popay T, Bermingham DP, Freeman P, Wright J, Blakely RD.
Dopamine-dependent, swimming-induced paralysis arises as a consequence of loss of function mutations in the RUNX transcription factor RNT-1.
PLoS One 2019 14(5) e0216417 
[ PubMed ID = 31083672 ] [ RRC reference ]