Mutants (Isolated)


Allele Nametm2044
Sequence NameT14F9.5
CGC Namelin-32
Worm BaseAllele Name tm2044
CGC Name lin-32
Sequence T14F9.5
Phenotypehomozygous viable. Dr. D. Portman: strong ray-missing phenotype. Dr. O. Hobert: Nat. Meth.5, 869 (2008).
Mutation site24537/24538-TCTTAC-25636/25637 (1099 bp deletion + 6 bp insertion)
Putative gene structurecomplement(join(24191..24337, 24722..24860, 24926..25068))
Map position-16.75
Map position of balancer
Distributed lab
DepositorDr. S. Mitani
References Please submit your publication
Doitsidou M, Flames N, Lee AC, Boyanov A, Hobert O.
Automated screening for mutants affecting dopaminergic-neuron specification in C. elegans.
Nat. Methods 2008 5(10) 869-72 
[ PubMed ID = 18758453 ] [ RRC reference ]

Miller RM, Portman DS.
The Wnt/beta-catenin asymmetry pathway patterns the atonal ortholog lin-32 to diversify cell fate in a Caenorhabditis elegans sensory lineage.
J. Neurosci. 2011 31(37) 13281-91 
[ PubMed ID = 21917811 ] [ RRC reference ]

Hori S, Oda S, Suehiro Y, Iino Y, Mitani S.
OFF-responses of interneurons optimize avoidance behaviors depending on stimulus strength via electrical synapses.
PLoS Genet. 2018 14(6) e1007477 
[ PubMed ID = 29939997 ] [ RRC reference ]