WormBase Tree Display for Gene: WBGene00004854
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| WBGene00004854 | SMap | S_parent | Sequence | CHROMOSOME_X | |||
|---|---|---|---|---|---|---|---|
| Identity (6) | |||||||
| Gene_info | Biotype | SO:0001217 | |||||
| Gene_class | slt | ||||||
| Allele (191) | |||||||
| Strain | WBStrain00034914 | ||||||
| WBStrain00005267 | |||||||
| WBStrain00005270 | |||||||
| WBStrain00005271 | |||||||
| WBStrain00005272 | |||||||
| RNASeq_FPKM (74) | |||||||
| GO_annotation (26) | |||||||
| Ortholog (37) | |||||||
| Paralog | WBGene00007261 | Caenorhabditis elegans | From_analysis | WormBase-Compara | |||
| WBGene00013542 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||
| WBGene00020693 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||
| WBGene00022129 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||
| Structured_description (2) | |||||||
| Disease_info | Potential_model | DOID:13207 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:11086) | ||
| DOID:0080745 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:11086) | ||||
| DOID:10223 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:11086) | ||||
| DOID:0060224 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:11086) | ||||
| Molecular_info | Corresponding_CDS | F40E10.4 | |||||
| Corresponding_CDS_history | F40E10.4:wp90 | ||||||
| Corresponding_transcript | F40E10.4.1 | ||||||
| Other_sequence (11) | |||||||
| Associated_feature | WBsf648747 | ||||||
| WBsf648748 | |||||||
| WBsf663583 | |||||||
| WBsf663584 | |||||||
| WBsf663585 | |||||||
| WBsf717401 | |||||||
| WBsf236701 | |||||||
| WBsf236702 | |||||||
| WBsf236703 | |||||||
| Experimental_info (7) | |||||||
| Map_info | Map | X | Position | 19.7628 | Error | 0.06206 | |
| Positive | Positive_clone | F40E10 | Inferred_automatically | From CDS info | |||
| From sequence, transcript, pseudogene data | |||||||
| Mapping_data | Multi_point | 4664 | |||||
| 5528 | |||||||
| Pseudo_map_position | |||||||
| Reference (74) | |||||||
| 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 |
