| Allele Name | tm700 |
| Allele Type | Normal |
| Sequence Name | C09B8.6 |
| Gene Name | hsp-25 |
| Worm Base | Allele Name |
tm700
|
| Gene Name |
hsp-25
|
| Sequence |
C09B8.6
|
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)
| 32112/32113-32982/32983 (870 bp deletion) |
| Chromosome | X |
| Putative gene structure | complement(join(28985..29095, 29218..29341, 29907..30012, 31795..31932, 33332..33474, 33664..33701)) |
| Map position | -3.82 |
| Balancer | |
| Map position of balancer | |
| Sequence of primers | ExtFwd:TCCGAATCCACCAGTACGGT,IntFwd:GGTTCGAAGTCTCGTGGTGA,ExtRev:ACTACTGTTGGTTGGAAGGA,IntRev:CGATCATCTAGTCGGAAGAA |
| Distributed lab | |
| Depositor | Dr. S. Mitani/NBRP |
| References |
Please submit your publication
Soh MS, Cheng X, Vijayaraghavan T, Vernon A, Liu J, Neumann B.
Disruption of genes associated with Charcot-Marie-Tooth type 2 lead to common behavioural, cellular and molecular defects in Caenorhabditis elegans.
PLoS One 2020 15(4) e0231600
[ PubMed ID = 32294113 ]
[ RRC reference ]
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