| Allele Name | tm5861 |
| Balance | Not Required |
| OutCross | Not Accepted |
| Sequence Name | R151.6 |
| Gene Name | R151.6 |
| Worm Base | Allele 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) |
| Chromosome | III |
| Putative gene structure | complement(join(24567..24763, 24860..25058, 25262..25492, 25575..25631)) |
| Map position | -0.77 |
| Balancer | |
| Map position of balancer | |
| Sequence of primers | IntFwd:ATATACAAGCCACTGTGGAG,ExtRev:GATCTGTTGAACCTGTGCCT,IntRev:ACCTGTGCCTTTTCCCATAC,ExtFwd:AGGTTCCGGTCGGCGTTCAT |
| 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 ]
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