WormBase Tree Display for Gene: WBGene00004969
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| WBGene00004969 | SMap | S_parent | Sequence | CHROMOSOME_I | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 1 | |||||||
| Name | CGC_name | spe-15 | Person_evidence | WBPerson252 | |||||
| Sequence_name | F47G6.4 | ||||||||
| Molecular_name | F47G6.4a | ||||||||
| F47G6.4a.1 | |||||||||
| CE17841 | |||||||||
| F47G6.4b | |||||||||
| CE49560 | |||||||||
| F47G6.4c | |||||||||
| CE49613 | |||||||||
| F47G6.4b.1 | |||||||||
| F47G6.4c.1 | |||||||||
| Other_name | hum-3 | ||||||||
| CELE_F47G6.4 | Accession_evidence | NDB | BX284601 | ||||||
| Public_name | spe-15 | ||||||||
| DB_info | Database | AceView | gene | 1B937 | |||||
| WormQTL | gene | WBGene00004969 | |||||||
| WormFlux | gene | WBGene00004969 | |||||||
| NDB | locus_tag | CELE_F47G6.4 | |||||||
| Panther | gene | CAEEL|WormBase=WBGene00004969|UniProtKB=Q9TZI9 | |||||||
| family | PTHR13140 | ||||||||
| NCBI | gene | 171712 | |||||||
| RefSeq | protein | NM_001306501.3 | |||||||
| NM_001306502.3 | |||||||||
| NM_058455.6 | |||||||||
| TrEMBL | UniProtAcc | Q9TZI9 | |||||||
| W6RY57 | |||||||||
| W6RRZ0 | |||||||||
| UniProt_GCRP | UniProtAcc | Q9TZI9 | |||||||
| OMIM | gene | 600970 | |||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 07 Apr 2004 11:29:37 | WBPerson1971 | Event | Imported | Initial conversion from geneace | ||
| Status | Live | ||||||||
| Gene_info (11) | |||||||||
| Disease_info | Potential_model | DOID:0110495 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:7605) | ||||
| DOID:10283 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:7605) | ||||||
| DOID:10003 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:7605) | ||||||
| DOID:0110552 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:7605) | ||||||
| DOID:2394 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:7605) | ||||||
| Molecular_info | Corresponding_CDS | F47G6.4a | |||||||
| F47G6.4b | |||||||||
| F47G6.4c | |||||||||
| Corresponding_transcript | F47G6.4a.1 | ||||||||
| F47G6.4b.1 | |||||||||
| F47G6.4c.1 | |||||||||
| Other_sequence (64) | |||||||||
| Associated_feature | WBsf655927 | ||||||||
| WBsf655928 | |||||||||
| WBsf980943 | |||||||||
| WBsf982702 | |||||||||
| WBsf982703 | |||||||||
| WBsf982704 | |||||||||
| WBsf982705 | |||||||||
| WBsf1009217 | |||||||||
| WBsf1009218 | |||||||||
| WBsf1009219 | |||||||||
| Experimental_info | RNAi_result (11) | ||||||||
| Expr_pattern | Expr15151 | ||||||||
| Expr1025757 | |||||||||
| Expr1032472 | |||||||||
| Expr1151530 | |||||||||
| Expr2016033 | |||||||||
| Expr2034268 | |||||||||
| Antibody | WBAntibody00002868 | ||||||||
| Microarray_results (24) | |||||||||
| Expression_cluster (226) | |||||||||
| Interaction (27) | |||||||||
| WBProcess | WBbiopr:00000069 | ||||||||
| Map_info | Map | I | Position | -14.673 | Error | 0.007182 | |||
| Well_ordered | |||||||||
| Positive | Positive_clone | F47G6 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Mapping_data | 2_point | 693 | |||||||
| Multi_point | 1050 | ||||||||
| 4668 | |||||||||
| Pos_neg_data | 3186 | ||||||||
| Reference (15) | |||||||||
| Remark | [Titus MA] hum-3 deletion mutant (ok153) is allelic to spe-15(hc75). Both mutant strains exhibit defective asymmetric sorting of mitochondria, FB/MOs, actin and microtubules during the budding of spermatids from secondary spermatocytes. | ||||||||
| Method | Gene |
