WormBase Tree Display for Variation: WBVar00144802
expand all nodes | collapse all nodes | view schema
WBVar00144802 | Evidence | Paper_evidence | WBPaper00012673 | ||||||
---|---|---|---|---|---|---|---|---|---|
Name | Public_name | e2394 | |||||||
Sequence_details | SeqStatus | Pending_curation | |||||||
Variation_type | Allele | ||||||||
Origin | Species | Caenorhabditis elegans | |||||||
Laboratory | CB | ||||||||
Status | Live | ||||||||
Affects | Gene | WBGene00001194 | |||||||
Description | Phenotype | WBPhenotype:0000062 | Paper_evidence | WBPaper00003450 | |||||
Curator_confirmed | WBPerson2987 | ||||||||
Remark | egl-27(e2394) animals exhibited an 11% penetrant embryonic or L1 larval arrest (Table 1) | Paper_evidence | WBPaper00003450 | ||||||
Curator_confirmed | WBPerson2987 | ||||||||
Penetrance | Incomplete | 11% penetrant | Paper_evidence | WBPaper00003450 | |||||
Curator_confirmed | WBPerson2987 | ||||||||
WBPhenotype:0000816 | Paper_evidence | WBPaper00003450 | |||||||
Curator_confirmed | WBPerson2987 | ||||||||
Remark | Approximately 40% of egl-27(e2394) animals exhibited missing QL and/or QR neuroblasts at hatching (Table 1) | Paper_evidence | WBPaper00003450 | ||||||
Curator_confirmed | WBPerson2987 | ||||||||
Penetrance | Incomplete | 40% penetrant | Paper_evidence | WBPaper00003450 | |||||
Curator_confirmed | WBPerson2987 | ||||||||
EQ_annotations | Anatomy_term | WBbt:0004056 | PATO:0000460 | Paper_evidence | WBPaper00003450 | ||||
Curator_confirmed | WBPerson2987 | ||||||||
WBbt:0004054 | PATO:0000460 | Paper_evidence | WBPaper00003450 | ||||||
Curator_confirmed | WBPerson2987 | ||||||||
Life_stage | WBls:0000024 | PATO:0000460 | Paper_evidence | WBPaper00003450 | |||||
Curator_confirmed | WBPerson2987 | ||||||||
WBPhenotype:0000828 | Paper_evidence | WBPaper00003450 | |||||||
Curator_confirmed | WBPerson2987 | ||||||||
Remark | egl-27(e2394) mutants exhibited an abnormal pattern of T cell lineages, with all descendants of T adopting a hypodermal or hypodermal-like fate, unlike wild type (Figure 1). | Paper_evidence | WBPaper00003450 | ||||||
Curator_confirmed | WBPerson2987 | ||||||||
EQ_annotations | Anatomy_term | WBbt:0006994 | PATO:0000460 | Paper_evidence | WBPaper00003450 | ||||
Curator_confirmed | WBPerson2987 | ||||||||
WBbt:0006996 | PATO:0000460 | Paper_evidence | WBPaper00003450 | ||||||
Curator_confirmed | WBPerson2987 | ||||||||
WBbt:0006995 | PATO:0000460 | Paper_evidence | WBPaper00003450 | ||||||
Curator_confirmed | WBPerson2987 | ||||||||
WBbt:0006997 | PATO:0000460 | Paper_evidence | WBPaper00003450 | ||||||
Curator_confirmed | WBPerson2987 | ||||||||
WBPhenotype:0002211 | Paper_evidence | WBPaper00003450 | |||||||
Curator_confirmed | WBPerson2987 | ||||||||
Remark | The egl-27(e2394) mutation results in a completely penetrant phasmid dye filling defect, indicative of abnormal T cell polarity (Table 1). | Paper_evidence | WBPaper00003450 | ||||||
Curator_confirmed | WBPerson2987 | ||||||||
Penetrance | Complete | Paper_evidence | WBPaper00003450 | ||||||
Curator_confirmed | WBPerson2987 | ||||||||
EQ_annotations | Anatomy_term | WBbt:0005425 | PATO:0000460 | Paper_evidence | WBPaper00003450 | ||||
Curator_confirmed | WBPerson2987 | ||||||||
Reference | WBPaper00012673 | ||||||||
WBPaper00003450 | |||||||||
Method | Allele |