分離済み変異体

tm5861

Allele Nametm5861
BalanceNot Required
OutCrossNot Accepted
Sequence NameR151.6
Gene NameR151.6
Worm BaseAllele Name tm5861
Gene Name R151.6
Sequence R151.6
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) 25251/25252-25750/25751 (499 bp deletion)
ChromosomeIII
Putative gene structurecomplement(join(24567..24763, 24860..25058, 25262..25492, 25575..25631))
Map position-0.77
Balancer
Map position of balancer
Sequence of primersIntFwd:ATATACAAGCCACTGTGGAG,ExtRev:GATCTGTTGAACCTGTGCCT,IntRev:ACCTGTGCCTTTTCCCATAC,ExtFwd:AGGTTCCGGTCGGCGTTCAT
Distributed lab
DepositorDr. 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 ]