| Allele Name | tm3912 |
| Balance | Not Required |
| OutCross | Not Accepted |
| Sequence Name | F38A5.7 |
| Gene Name | F38A5.7 |
| Worm Base | Allele Name |
tm3912
|
| Gene Name |
F38A5.7
|
| Sequence |
F38A5.7
|
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)
| 21580/21581-21786/21787 (206 bp deletion) |
| Chromosome | IV |
| Putative gene structure | join(21727..21840,21901..22296) |
| Map position | 3.21 |
| Balancer | |
| Map position of balancer | |
| Sequence of primers | IntRev:TTACGAGGGGATCGGATCTA,IntFwd:GCGTCGCGCAATACTCATAG,ExtRev:GCAGTGGGAGATCAGAGCAA,ExtFwd:CTGCGTAGCACACCTCCTTC |
| Distributed lab | |
| Depositor | Dr. S. Mitani/NBRP |
| References |
Please submit your publication
Polley SR, Kuzmanov A, Kuang J, Karpel J, Lažetić V, Karina EI, Veo BL, Fay DS. Implicating SCF complexes in organogenesis in Caenorhabditis elegans. Genetics 2014 196(1) 211-23
[ PubMed ID = 24214340 ]
[ RRC reference ]
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