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Gene: F11C1.6 
| F11C1.6 | Evidence | Paper_evidence | WBPaper00003416 | ||||||
|---|---|---|---|---|---|---|---|---|---|
| WBPaper00004124 | |||||||||
| WBPaper00004329 | |||||||||
| SMap | S_parent | Sequence | F11C1 | ||||||
| Chromosome | X | ||||||||
| Identity | Version | 1 | |||||||
| Name (7) | |||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 07 Apr 2004 11:29:32 | WBPerson1971 | Event | Imported | Initial conversion from geneace | ||
| Status | Live | ||||||||
| Gene_info | Gene_class | nhr | |||||||
| Allele | jm2389 | Inferred_automatically | From strain object: HL2000 | ||||||
| ok645 | Inferred_automatically | From strain object: VC469 | |||||||
| ku217 | Paper_evidence | WBPaper00024419 | |||||||
| Phenotype | [M Asahina] jm2389 is mutagenized using TMP/UV and detected a deletion by PCR. This removes the coding region from Gly40 in the P-box of the first zinc finger motif to Ser377 in the middle of the conserved region II within the LBD (ref. Asahina M et al. 2000 The conserved nuclear receptor Ftz-F1 is required for embryogenesis, moulting and reproduction in Caenorhabditis elegans. Genes to Cells 5: 711). Phenotype is homozygous embryonic lethal at 1.5-fold to 2-fold stage. Balanced with +/szT1[lon-2(e678)] I; nDf19/szT1 X (strain MT1401) | ||||||||
| Strain | HL2000 | ||||||||
| VC469 | |||||||||
| GO_term (6) | |||||||||
| Structured_description (2) | |||||||||
| Molecular_info (5) | |||||||||
| Experimental_info | RNAi_result (7) | ||||||||
| WB_RNAi_result (14) | |||||||||
| Expr_pattern (7) | |||||||||
| Reference | WBPaper00004124 | ||||||||
| WBPaper00023160 | |||||||||
| WBPaper00004329 | |||||||||
| WBPaper00004438 | |||||||||
| WBPaper00005654 | |||||||||
| WBPaper00006295 | |||||||||
| WBPaper00006370 | |||||||||
| WBPaper00006399 | |||||||||
| WBPaper00006412 | |||||||||
| WBPaper00010604 | |||||||||
| WBPaper00011606 | |||||||||
| WBPaper00017764 | |||||||||
| WBPaper00018194 | |||||||||
| WBPaper00018680 | |||||||||
| WBPaper00023159 | |||||||||
| WBPaper00024664 | |||||||||
| WBPaper00024419 | |||||||||
| WBPaper00024002 | |||||||||
| WBPaper00017650 | |||||||||
| WBPaper00005046 | |||||||||
| WBPaper00024128 | |||||||||
| WBPaper00005201 | |||||||||
| WBPaper00025190 | |||||||||
| WBPaper00025610 | |||||||||
| WBPaper00025032 | |||||||||
| WBPaper00026627 | |||||||||
| WBPaper00024393 | |||||||||
| Remark | Map position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC. | CGC_data_submission | |||||||
| Method | Gene |
