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分離済み変異体

Allele Name		tm5913
Balance		Completed
OutCross		Not Accepted
Sequence Name		F59G1.7
Gene Name		frh-1
Worm Base	Allele Name	tm5913 (x1)
	Gene Name	frh-1
	Sequence	F59G1.7
Phenotype Information from the receiver is posted in the form of a "researcher : phenotype"		lethal or sterile
Mutation site Please see gene structure to locate the deletion in relation to exon(s)		21291/21292-21642/21643 (351 bp deletion)
Chromosome		II
Putative gene structure		join(21324..21534, 21581..21677, 21929..22031)
Map position		-0.85
Balancer		mIn1 [e128 mIs14]
Map position of balancer
Sequence of primers		ExtFwd:TACCCGGTCTCGACGACACA,IntFwd:CGGTCTCGACGACACATCAT,ExtRev:TCGTGAATCTGAATCCGTCA,IntRev:CCGGATTAGACATGTCGCGA
Distributed lab
Depositor		Dr. S. Mitani/NBRP
References		Please submit your publication Meisel JD, Joshi PR, Spelbring AN, Wang H, Wellner SM, Wiesenthal PP, Miranda M, McCoy JG, Barondeau DP, Ruvkun G, Mootha VK. Mutations in mitochondrial ferredoxin FDX2 suppress frataxin deficiency. Nature 2026 649(8097) 713-720  [ PubMed ID = 41372402 ] [ RRC reference ] Ast T, Meisel JD, Patra S, Wang H, Grange RMH, Kim SH, Calvo SE, Orefice LL, Nagashima F, Ichinose F, Zapol WM, Ruvkun G, Barondeau DP, Mootha VK. Hypoxia Rescues Frataxin Loss by Restoring Iron Sulfur Cluster Biogenesis. Cell 2019 177(6) 1507-1521.e16  [ PubMed ID = 31031004 ] [ RRC reference ]