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分離済み変異体

Allele Name		tm4623
Balance		Not Required
OutCross		Not Accepted
Sequence Name		C33C12.8
Gene Name		C33C12.8
Worm Base	Allele Name	tm4623
	Gene Name	C33C12.8
	Sequence	C33C12.8
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)		23683/23684-24167/24168 (484 bp deletion)
Chromosome		II
Putative gene structure		complement(join(21872..22103, 22613..22776, 22824..22904, 23005..23136, 23405..23742, 24069..24141, 24184..24317, 24717..24869, 24920..25258, 25736..25775))
Map position		-13.84
Balancer
Map position of balancer
Sequence of primers		ExtFwd:CGACCGCAACGCAAGTCCAA,IntFwd:AACTCACAGTGTCTGCCCAT,ExtRev:CCGATGCTTCTGGTGCGAAT,IntRev:GGCTGATACAATTCTGAGAC
Distributed lab
Depositor		Dr. S. Mitani
References		Please submit your publication Liu N, Li R, Huang X, Lakso M, Wong G. The C. elegans gba-3 gene encodes a glucocerebrosidase that exacerbates α-synuclein-mediated impairments in deletion mutants. Transl Neurodegener 2025 14(1) 9  [ PubMed ID = 39940047 ] [ RRC reference ]