WormMine

WSWS298

An integrated data resource for C. elegans and related nematodes

Phenotype : WBPhenotype:0000744 transgene induced cosuppression variant

Description  Animals exhibit variations in the silencing of endogenous genes after introduction of repetitive exogenous cognate DNA compared to control.
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68 RNAi

WormBase ID
WBRNAi00069421
WBRNAi00069437
WBRNAi00069447
WBRNAi00069456
WBRNAi00069481
WBRNAi00069464
WBRNAi00069425
WBRNAi00069448
WBRNAi00069450
WBRNAi00069453
WBRNAi00069452
WBRNAi00069455
WBRNAi00069454
WBRNAi00069459
WBRNAi00069460
WBRNAi00069462
WBRNAi00069468
WBRNAi00069419
WBRNAi00069420
WBRNAi00069423
WBRNAi00069422
WBRNAi00069424
WBRNAi00069427
WBRNAi00069426
WBRNAi00069429
WBRNAi00069428
WBRNAi00069431
WBRNAi00069430
WBRNAi00069433
WBRNAi00069432

0 RNAi Not Observed

0 Children

1 Data Sets

Name URL
WormBaseAcedbConverter  

1 Parents

Identifier Name Description
WBPhenotype:0002063 maintenance of gene silencing variant Animals differ from controls in the expression of genes targeted for silencing (gene inactivation) in subsequent generations via transcriptional or post-transcriptional processes.

0 Phenotype Allele

2 Phenotype Allele Not Observed

Public Name
tm1102
tm1341

1 Synonyms

Name Type
transgene induced cosuppression abnormal