WormBase Tree Display for Gene: WBGene00006788
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| WBGene00006788 | SMap | S_parent | Sequence | CHROMOSOME_II | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 1 | |||||||
| Name | CGC_name | unc-53 | Person_evidence | WBPerson261 | |||||
| Sequence_name | F45E10.1 | ||||||||
| Molecular_name (24) | |||||||||
| Other_name | CELE_F45E10.1 | Accession_evidence | NDB | BX284602 | |||||
| Public_name | unc-53 | ||||||||
| DB_info | Database (11) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 07 Apr 2004 11:29:42 | WBPerson1971 | Event | Imported | Initial conversion from geneace | ||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | unc | ||||||||
| Reference_allele | WBVar00143183 | ||||||||
| Allele (424) | |||||||||
| Legacy_information | e404 : sluggish poor backing dumpyish somewhat Egl; males have abnormal bursal anatomy. ES2 ME0. NA4 (n152 n166 n569). | ||||||||
| See also e2432, e2499, n152, n166, n569 | |||||||||
| [C.elegansII] e404 : sluggish, poor backing, dumpyish; somewhat Egl; multiple defects in neuronal outgrowth, branching; also defects in excretory canal extension, gonad arm growth; males have abnormal bursal anatomy. ES2 ME0. OA>5: n152, n166, n569 (synergizes with sem-5(n177) to give strong Sem migration defect),e2432, e2499, etc. Null phenotype uncertain; some lethality in strong alleles. Cloned: multiple transcripts (different 5' ends); one encodes 1528 aa protein, predicted to bind actin, ATP/GTP; may interact with SEM-5. Transgene overexpression leads to extension of growth cones along a-p axis. [Hedgecock et al. 1987; Hekimi and Kershaw 1993; UG] | |||||||||
| Strain | WBStrain00026706 | ||||||||
| WBStrain00026870 | |||||||||
| WBStrain00032757 | |||||||||
| WBStrain00034470 | |||||||||
| WBStrain00034483 | |||||||||
| WBStrain00037045 | |||||||||
| WBStrain00004162 | |||||||||
| WBStrain00004572 | |||||||||
| WBStrain00005655 | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation (21) | |||||||||
| Ortholog (46) | |||||||||
| Structured_description (2) | |||||||||
| Disease_info | Potential_model | DOID:2559 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:15998) | ||||
| Molecular_info | Corresponding_CDS | F45E10.1a | |||||||
| F45E10.1b | |||||||||
| F45E10.1c | |||||||||
| F45E10.1d | |||||||||
| F45E10.1e | |||||||||
| F45E10.1f | |||||||||
| F45E10.1g | |||||||||
| F45E10.1h | |||||||||
| Corresponding_CDS_history | F45E10.1:wp82 | ||||||||
| Corresponding_transcript | F45E10.1a.1 | ||||||||
| F45E10.1b.1 | |||||||||
| F45E10.1c.1 | |||||||||
| F45E10.1d.1 | |||||||||
| F45E10.1e.1 | |||||||||
| F45E10.1f.1 | |||||||||
| F45E10.1g.1 | |||||||||
| F45E10.1h.1 | |||||||||
| Other_sequence (27) | |||||||||
| Associated_feature (66) | |||||||||
| Experimental_info | RNAi_result (14) | ||||||||
| Expr_pattern (12) | |||||||||
| Drives_construct (25) | |||||||||
| Construct_product | WBCnstr00009444 | ||||||||
| WBCnstr00010519 | |||||||||
| WBCnstr00010520 | |||||||||
| WBCnstr00010521 | |||||||||
| WBCnstr00034150 | |||||||||
| Antibody | WBAntibody00001615 | ||||||||
| WBAntibody00001625 | |||||||||
| Microarray_results (40) | |||||||||
| Expression_cluster (219) | |||||||||
| Interaction (103) | |||||||||
| Anatomy_function | WBbtf0113 | ||||||||
| WBbtf0114 | |||||||||
| WBbtf0118 | |||||||||
| WBbtf0119 | |||||||||
| Map_info | Map | II | Position | 3.16568 | Error | 0.005694 | |||
| Well_ordered | |||||||||
| Positive | Positive_clone | F45E10 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| T28D2 | |||||||||
| Mapping_data | 2_point | 43 | |||||||
| Multi_point (11) | |||||||||
| Pos_neg_data | 2145 | ||||||||
| 2146 | |||||||||
| 2159 | |||||||||
| 2163 | |||||||||
| 4533 | |||||||||
| 4534 | |||||||||
| 4535 | |||||||||
| 4536 | |||||||||
| 4539 | |||||||||
| 10562 | |||||||||
| Reference (99) | |||||||||
| Method | Gene |
