分離済み変異体

tm795

Allele Nametm795
BalanceNot Required
OutCrossNot Accepted
Sequence NameF30A10.8a
Gene Namestn-1
Worm BaseAllele Name tm795
Gene Name stn-1
Sequence F30A10.8a
Phenotype Information from the receiver is posted in the form of a "researcher : phenotype" homozygous viable. Dr. P. Roy: no muscle arm phenotype.
Mutation site Please see gene structure to locate the deletion in relation to exon(s) 31288/31289-31719/31720 (431 bp deletion)
ChromosomeI
Putative gene structurejoin(29443..29538, 30997..31118, 31560..32475, 32587..32682, 32849..32941)
Map position3.78
Balancer
Map position of balancer
Sequence of primersIntRev:CGCGTACAATCCTAATCGAT,ExtFwd:GGCTGAAGCAGAGAAACGGA,ExtRev:GAGCTCCAATGAACTAACCT,IntFwd:CGGACAGTTCGAGTTGTGAA
Distributed lab
DepositorDr. S. Mitani/NBRP
References Please submit your publication
Oh KH, Abraham LS, Gegg C, Silvestri C, Huang YC, Alkema MJ, Furst J, Raicu D, Kim H.
Presynaptic BK channel localization is dependent on the hierarchical organization of alpha-catulin and dystrobrevin and fine-tuned by CaV2 calcium channels.
BMC Neurosci 2015 16 26 
[ PubMed ID = 25907097 ] [ RRC reference ]

Abraham LS, Oh HJ, Sancar F, Richmond JE, Kim H.
An alpha-catulin homologue controls neuromuscular function through localization of the dystrophin complex and BK channels in Caenorhabditis elegans.
PLoS Genet 2010 6(8)  
[ PubMed ID = 20865173 ] [ RRC reference ]