分離済み変異体

tm3779

Allele Nametm3779
BalanceNot Required
OutCrossNot Accepted
Sequence NameF17H10.3
Gene Namesnx-17
Worm BaseAllele Name tm3779
Gene Name snx-17
Sequence F17H10.3
Phenotype Information from the receiver is posted in the form of a "researcher : phenotype" homozygous viable. Dr. Z. Zhou: no persistent cell corpses.
Mutation site Please see gene structure to locate the deletion in relation to exon(s) 12004/12005-ATAATTTTTTC-12547/12548 (544 bp deletion + 11 bp insertion)
ChromosomeX
Putative gene structurecomplement(join(10053..10109, 10169..10279, 10462..10599, 10646..10786, 10834..10974, 11161..11332, 11381..11480, 11534..11663, 11993..12103, 12157..12221, 12267..12462, 12602..12736, 15676..15801))
Map position10.23
Balancer
Map position of balancer
Sequence of primersExtFwd:CGTAGGAGTATGTCGAGAGT,IntFwd:TGCGGAGGAACTGTAACTAA,ExtRev:CCAGCGGATAAGACAACGTT,IntRev:CCGGATACGAAGACACTAGT
Distributed lab
DepositorDr. S. Mitani/NBRP
References Please submit your publication
Vieira N, Bessa C, Rodrigues AJ, Marques P, Chan FY, de Carvalho AX, Correia-Neves M, Sousa N.
Sorting nexin 3 mutation impairs development and neuronal function in Caenorhabditis elegans.
Cell Mol Life Sci 2018 75(11) 2027-2044 
[ PubMed ID = 29196797 ] [ RRC reference ]