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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