| Allele Name | tm4853 |
| Sequence Name | C36A4.9 |
| CGC Name | acs-19 |
| Worm Base | Allele Name |
tm4853
|
| CGC Name |
acs-19
|
| Sequence |
C36A4.9
|
| Phenotype | homozygous viable. |
| Mutation site | 36972/36973-37442/37443 (470 bp deletion) |
| Chromosome | III |
| Putative gene structure | join(35919..35978, 36029..36739, 36864..36979, 37038..37364, 37416..38244) |
| Map position | -42.5 |
| Balancer | |
| Map position of balancer | |
| Sequence of primers | IntRev:GTCTGGCACCATCTCCAGTG,ExtRev:CGTCCAGTTATCCACAAGTA,IntFwd:ACCTAGCCAACGATGGAGAA,ExtFwd:CATGTCGGACGTTCGCGTCA |
| Distributed lab | |
| Depositor | Dr. S. Mitani/NBRP |
| References |
Please submit your publication
Segref A, Kevei É, Pokrzywa W, Schmeisser K, Mansfeld J, Livnat-Levanon N, Ensenauer R, Glickman MH, Ristow M, Hoppe T.
Pathogenesis of human mitochondrial diseases is modulated by reduced activity of the ubiquitin/proteasome system.
Cell Metab. 2014 19(4) 642-52
[ PubMed ID = 24703696 ]
[ RRC reference ]
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