WormBase Tree Display for Gene: WBGene00001501
expand all nodes | collapse all nodes | view schema
| WBGene00001501 | SMap | S_parent | Sequence | D1037 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 1 | |||||||
| Name | CGC_name | ftn-2 | |||||||
| Sequence_name | D1037.3 | ||||||||
| Molecular_name | D1037.3 | ||||||||
| D1037.3.1 | |||||||||
| CE20622 | |||||||||
| Other_name | CELE_D1037.3 | Accession_evidence | NDB | BX284601 | |||||
| Public_name | ftn-2 | ||||||||
| DB_info | Database (12) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 07 Apr 2004 11:29:24 | WBPerson1971 | Event | Imported | Initial conversion from geneace | ||
| Status | Live | ||||||||
| Gene_info (9) | |||||||||
| Disease_info | Potential_model | DOID:0111256 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:3999) | ||||
| DOID:1289 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:3999) | ||||||
| DOID:0111031 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:3976) | ||||||
| DOID:0080600 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:3976,HGNC:3999) | ||||||
| DOID:0110737 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:3999) | ||||||
| DOID:679 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:3999) | ||||||
| Molecular_info | Corresponding_CDS | D1037.3 | |||||||
| Corresponding_transcript | D1037.3.1 | ||||||||
| Other_sequence (155) | |||||||||
| Associated_feature (16) | |||||||||
| Experimental_info (9) | |||||||||
| Map_info | Map | I | Position | -2.93309 | Error | 0.018064 | |||
| Positive | Positive_clone | D1037 | Inferred_automatically | From CDS info | |||||
| From sequence, transcript, pseudogene data | |||||||||
| Mapping_data | Multi_point | 4327 | |||||||
| 4429 | |||||||||
| 4670 | |||||||||
| Pseudo_map_position | |||||||||
| Reference (21) | |||||||||
| 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 |
