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分離済み変異体

Allele Name		tm4671
Balance		Not Required
OutCross		Not Accepted
Sequence Name		C18H9.3
Gene Name		C18H9.3
Worm Base	Allele Name	tm4671
	Gene Name	C18H9.3
	Sequence	C18H9.3
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)		8981/8982-9457/9458 (476 bp deletion)
Chromosome		II
Putative gene structure		join(6768..6823, 7224..7320, 8307..8475, 8549..8785, 8867..9580, 9627..10813, 10863..11159)
Map position		-0.04
Balancer
Map position of balancer
Sequence of primers		ExtFwd:GATATGGAGCCGCTTCCGGA,IntFwd:AGTCGCTGGGCTCCGAAATC,ExtRev:ACGTGCCTCAAGTTCCGCTC,IntRev:TCACACGATCCCGTCGAATC
Distributed lab
Depositor		Dr. S. Mitani/NBRP
References		Please submit your publication McDiarmid TA, Belmadani M, Liang J, Meili F, Mathews EA, Mullen GP, Hendi A, Wong WR, Rand JB, Mizumoto K, Haas K, Pavlidis P, Rankin CH. Systematic phenomics analysis of autism-associated genes reveals parallel networks underlying reversible impairments in habituation. Proc Natl Acad Sci U S A 2020 117(1) 656-667  [ PubMed ID = 31754030 ] [ RRC reference ]