分離済み変異体

tm4916

Allele Nametm4916
BalanceNot Required
OutCrossNot Accepted
Sequence NameD2013.3
Gene NameD2013.3
Worm BaseAllele Name tm4916
Gene Name D2013.3
Sequence D2013.3
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) 18781/18782-18952/18953 (171 bp deletion)
ChromosomeII
Putative gene structurecomplement(join(18080..18157, 18209..18509, 18565..18756, 18985..19218, 19263..19349, 19394..19540, 19821..19864))
Map position1.14
Balancer
Map position of balancer
Sequence of primersIntFwd:GTATCCTACCTCATAGCTTG,ExtRev:GTTCGTCACGAGGAGTACAT,ExtFwd:TGGTTGATCTGTCAAGGGAT,IntRev:GTCAGAAAACCAGACGGGTC
Distributed lab
DepositorDr. S. Mitani/NBRP
References Please submit your publication
Babu V, Hofmann K, Schumacher B.
A C. elegans homolog of the Cockayne syndrome complementation group A gene.
DNA Repair (Amst) 2014 24 57-62 
[ PubMed ID = 25453470 ] [ RRC reference ]