分離済み変異体

tm3160

Allele Nametm3160
BalanceNot Required
OutCrossNot Accepted
Sequence NameB0035.16
Gene NameB0035.16
Worm BaseAllele Name tm3160
Gene Name B0035.16
Sequence B0035.16
Phenotype Information from the receiver is posted in the form of a "researcher : phenotype" homozygous viable. Dr. C. Yang: normal cell death phenotype.
Mutation site Please see gene structure to locate the deletion in relation to exon(s) 947/948-1539/1540 (592 bp deletion)
ChromosomeIV
Putative gene structurecomplement(join(860..934, 1041..1259, 1305..1538, 1589..1761, 1808..1992, 2036..2178, 2494..2592))
Map position4.95
Balancer
Map position of balancer
Sequence of primersIntFwd:TCTCTCCTCCACCAAGGCAT,ExtFwd:GCCTCCTGCTGTTAATCAGT,ExtRev:GGTGCCGTAGGGTCTGTGTA,IntRev:GGGACATCACATTGTCCACG
Distributed lab
DepositorDr. S. Mitani/NBRP
References Please submit your publication
Navarro-González C, Moukadiri I, Villarroya M, López-Pascual E, Tuck S, Armengod ME.
Mutations in the Caenorhabditis elegans orthologs of human genes required for mitochondrial tRNA modification cause similar electron transport chain defects but different nuclear responses.
PLoS Genet 2017 13(7) e1006921 
[ PubMed ID = 28732077 ] [ RRC reference ]