WormBase Tree Display for RNAi: WBRNAi00088416
expand all nodes | collapse all nodes | view schema
WBRNAi00088416 | Homol | Homol_homol | F10G7:RNAi | |
---|---|---|---|---|
Sequence_info | DNA_text | ATGTTCTATGCACAGTTCGTTCTCGCCAAAAAGGGACCGTTGGCAAAAGTGTGGCTGGCAGCTCACTGGGAAAAAAAGCTGACAAAGGCGCAAATCTTCGAAACAGATGTTCCCCAAGCGATCGAGGAAGTCATTCGCCCCAAGGTTAAAATGGCGCTCCGAACAGTTGGACATCTTCTCCTTGGAATCGTGAGAATCTACTCGAAGAAGACACGATATCTTCTGGCTGATACAAATGAAGCGTATCAAAAGATGAAGATTAACTTCCGCAACGGATTCAGTTTTGAAGTCGACATTCCAGAGAATGCAGAAATTGAAGAGGATTTCTCAAACTTCATTGATAAGTACAATATCACAGTGCCCGAGTTCCACGATGCCGACTACAATGAGCAGCTCATTATGGCTAATGTGAGCCGTCGTGAAGACATCACCATGAAAGAAACCGTCAATTTCAATGTCGAGTTCAACATTGACGCAGATTTCGATGGGTTCGGTGACGAAGGAGAATCTTGGCAACTCGATCATCTCTACGGATCGGTGGAACCTTTGTCTTTGCGCCCCACTCCTCAGCCAGAATCGTTGATGGAAGTCGAACGAGATCGTGATGTGGCTGCAAATGGAACGGAAATTTCCCGTATAGATGCGGATAGTGTGATTTTCTCCGAAGGACCAACACGTCCAAATCTTATTTTTGACAATCAGGAAGGCGGAAATTTCATGCCTGAAATGAACCTGAAGGTTGAGAATCAAACACTGGAAAACGATGGTGGTGTTGGGCCTGCTGATATGTTCAGCTCAATGATTCATCCCGTCAGAGAGCATGCTGTCGCAGATGTTCAAAACGACGATGGTATGGACTTTGACTATCAACCGTTCGAGCCTGAAAACGTTGAGCCATCGAGACCACAAAGTCCCGAGTCATTTGCCCTGGAGCCTCTAGATGTGGAGCACATGGAAGGACGGAAAAAACGTCAGAGAAAAGCGAGAAAGCTGATTGTCGATGCTGAAACTATGATTTCAAACGACGCTTTCCGAGAGCAACAAGAAGACTTCTCCGATACGATGCGAGTAGTTGAAATGGCGCCTCCTACCAGAAAGATGTTCAATTTATGCGTCAGCGGAGATCTTCAACACCTCAGCCGTGAACCTGGATGCAAAATGTTCAACAGAGAACTCCTTCAAAGATACAGGAGATGTTTGGTCACCCGAGAGTTCGATCTCAATTACACCATGCAAGAGTTGAGCGATAGTTCGAGTTTCACTCCGTCAATGGAAGCTCAAGCTGAGCCATGGGAGGACTTGAACCTCAATGAGGACATTCAAGAAGATATTCAAGCGCAGGGACCAGCCGTTGATGAATTCTTTAATGATGTGCGCATGGATGATGATGATGACAGACAACCAGCTCAGGAAATGGACTTTGGTGACAACTTCGATTTTCCACAAGAAGTAGAACATCAAGAGTGTGCTCCGATCCCTATCCAGAGTGGATTCGCTGGAGAGAACAAAGAGAACGAGGACGCAGAGGATTGGTCTGATCCGTTCGGTTCTTCAAATTCCAGCAGACGTGGCCAGCTTGAAGCCTATGGATTCGGAAATACTTCGACCTACAAGGAAGACGATGGCAAATGGGCGAAACGCGCCAAGCACATTCTAAAGAAAGTCTCCGCGGATATTGAGACTTCGGGACAAGCGGACTTCTCATCTGTCACAGCAACTGCCAAGAATCGCAAGCAAGCTGCAGAGCAATTTTATTCGTTGCTTACCCTGGCCAAGTCTCAAGCAATAAGTGTTGATCAATCAGAGCCATACGGAGAGATCGTAATTCGTCCAGGAGCCAATTTCAAAGAAGCATGTCCACTGAGCTCTCCGAAACCGATGGGACTTGGAAATACAATGGAAAATTCCACTATGAGAACCCCAATGAGACCAGTTTAA | ||
Experiment | Laboratory | YM | ||
Date | 01 Jun 2003 00:00:00 | |||
Strain | WBStrain00000001 | |||
Temperature | 20 | |||
Delivered_by | Soaking | |||
Inhibits (3) | ||||
Species | Caenorhabditis elegans | |||
Reference | WBPaper00005937 | |||
Phenotype | WBPhenotype:0000050 | Remark | F1 embryos exhibited embryonic lethality with complete penetrance. Authors carefully observed the cell division process in scc-1/coh-2(RNAi) embryos, and found similar chromosome segregation defects in early cell cycles to the scc-3(RNAi), him-1/smc-1(RNAi), or smc-3(RNAi) embryos, although the penetrance was relatively low. This low penetrance (~10% of the RNAi-affected embryos) might be due to either gene-specific inefficiency of RNAi reaction or relatively high stability of the SCC-1/COH-2 protein compared with other cohesin components. The scc-1/coh-2(RNAi) embryos showed loose metaphase plates, asynchronous separation of chromosomes at anaphase, and formation of multiple nuclei after decondensation of chromosomes. | |
Penetrance | Complete | |||
WBPhenotype:0000059 | Remark | F1 embryos exhibited embryonic lethality with complete penetrance. Authors carefully observed the cell division process in scc-1/coh-2(RNAi) embryos, and found similar chromosome segregation defects in early cell cycles to the scc-3(RNAi), him-1/smc-1(RNAi), or smc-3(RNAi) embryos, although the penetrance was relatively low. This low penetrance (~10% of the RNAi-affected embryos) might be due to either gene-specific inefficiency of RNAi reaction or relatively high stability of the SCC-1/COH-2 protein compared with other cohesin components. The scc-1/coh-2(RNAi) embryos showed loose metaphase plates, asynchronous separation of chromosomes at anaphase, and formation of multiple nuclei after decondensation of chromosomes. | ||
WBPhenotype:0000688 | Remark | F1 embryos exhibited embryonic lethality with complete penetrance. Authors carefully observed the cell division process in scc-1/coh-2(RNAi) embryos, and found similar chromosome segregation defects in early cell cycles to the scc-3(RNAi), him-1/smc-1(RNAi), or smc-3(RNAi) embryos, although the penetrance was relatively low. This low penetrance (~10% of the RNAi-affected embryos) might be due to either gene-specific inefficiency of RNAi reaction or relatively high stability of the SCC-1/COH-2 protein compared with other cohesin components. The scc-1/coh-2(RNAi) embryos showed loose metaphase plates, asynchronous separation of chromosomes at anaphase, and formation of multiple nuclei after decondensation of chromosomes. | ||
WBPhenotype:0000697 | Remark | F1 embryos exhibited embryonic lethality with complete penetrance. Authors carefully observed the cell division process in scc-1/coh-2(RNAi) embryos, and found similar chromosome segregation defects in early cell cycles to the scc-3(RNAi), him-1/smc-1(RNAi), or smc-3(RNAi) embryos, although the penetrance was relatively low. This low penetrance (~10% of the RNAi-affected embryos) might be due to either gene-specific inefficiency of RNAi reaction or relatively high stability of the SCC-1/COH-2 protein compared with other cohesin components. The scc-1/coh-2(RNAi) embryos showed loose metaphase plates, asynchronous separation of chromosomes at anaphase, and formation of multiple nuclei after decondensation of chromosomes. | ||
WBPhenotype:0000773 | Remark | F1 embryos exhibited embryonic lethality with complete penetrance. Authors carefully observed the cell division process in scc-1/coh-2(RNAi) embryos, and found similar chromosome segregation defects in early cell cycles to the scc-3(RNAi), him-1/smc-1(RNAi), or smc-3(RNAi) embryos, although the penetrance was relatively low. This low penetrance (~10% of the RNAi-affected embryos) might be due to either gene-specific inefficiency of RNAi reaction or relatively high stability of the SCC-1/COH-2 protein compared with other cohesin components. The scc-1/coh-2(RNAi) embryos showed loose metaphase plates, asynchronous separation of chromosomes at anaphase, and formation of multiple nuclei after decondensation of chromosomes. | ||
Penetrance | Complete | |||
Remark | paper remark: Exact sequence used for RNAi not stated by authors, spliced coding region sequence of gene used for curation. Authors used yk256h5(scc-1/coh-2). | |||
Method | RNAi |