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分離済み変異体

Allele Name		tm1830
Balance		Not Required
OutCross		Not Accepted
Sequence Name		K04F10.2
Gene Name		K04F10.2
Worm Base	Allele Name	tm1830
	Gene Name	K04F10.2
	Sequence	K04F10.2
Phenotype Information from the receiver is posted in the form of a "researcher : phenotype"		homozygous viable. Dr. O. Blacque: normal dye filling and normal osmolarity sensing.
Mutation site Please see gene structure to locate the deletion in relation to exon(s)		29915/29916-30262/30263 (347 bp deletion)
Chromosome		I
Putative gene structure		join(28659..28756, 28800..28932, 29465..29632, 29689..30067, 30417..30564, 30617..30948, 31284..31394, 31442..31541, 31585..31726, 31780..31875)
Map position		1
Balancer
Map position of balancer
Sequence of primers		ExtFwd:CGGAGAGCAGTGAAGCCTGA,IntFwd:CCCGTATAGCTGTTACTTAC,ExtRev:CATCGGAAGTGGTCACTGTG,IntRev:GGCTATGTTCATCCACAAGT
Distributed lab
Depositor		Dr. S. Mitani/NBRP
References		Please submit your publication Sanders AA, de Vrieze E, Alazami AM, Alzahrani F, Malarkey EB, Sorusch N, Tebbe L, Kuhns S, van Dam TJ, Alhashem A, Tabarki B, Lu Q, Lambacher NJ, Kennedy JE, Bowie RV, Hetterschijt L, van Beersum S, van Reeuwijk J, Boldt K, Kremer H, Kesterson RA, Monies D, Abouelhoda M, Roepman R, Huynen MH, Ueffing M, Russell RB, Wolfrum U, Yoder BK, van Wijk E, Alkuraya FS, Blacque OE. KIAA0556 is a novel ciliary basal body component mutated in Joubert syndrome. Genome Biol 2015 16 293  [ PubMed ID = 26714646 ] [ RRC reference ]