WormBase Tree Display for Gene: WBGene00010701
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| WBGene00010701 | SMap | S_parent | Sequence | K09A9 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 2 | |||||||
| Name | CGC_name | ent-2 | Person_evidence | WBPerson1318 | |||||
| Sequence_name | K09A9.3 | ||||||||
| Molecular_name | K09A9.3 | ||||||||
| K09A9.3.1 | |||||||||
| CE11976 | |||||||||
| Other_name | CELE_K09A9.3 | Accession_evidence | NDB | BX284606 | |||||
| Public_name | ent-2 | ||||||||
| DB_info | Database (11) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 26 May 2004 16:54:51 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
| 2 | 04 Nov 2004 16:11:20 | WBPerson2970 | Name_change | CGC_name | ent-2 | ||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | ent | ||||||||
| Allele (59) | |||||||||
| Strain | WBStrain00036385 | ||||||||
| WBStrain00037923 | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation | 00086780 | ||||||||
| 00086781 | |||||||||
| 00086782 | |||||||||
| 00086783 | |||||||||
| 00086784 | |||||||||
| 00086785 | |||||||||
| 00118037 | |||||||||
| 00118038 | |||||||||
| 00118039 | |||||||||
| Ortholog (54) | |||||||||
| Paralog | WBGene00001320 | Caenorhabditis elegans | From_analysis | Inparanoid_8 | |||||
| Panther | |||||||||
| WormBase-Compara | |||||||||
| WBGene00008123 | Caenorhabditis elegans | From_analysis | Panther | ||||||
| WormBase-Compara | |||||||||
| WBGene00009499 | Caenorhabditis elegans | From_analysis | Panther | ||||||
| WormBase-Compara | |||||||||
| WBGene00009686 | Caenorhabditis elegans | From_analysis | Panther | ||||||
| WormBase-Compara | |||||||||
| WBGene00010510 | Caenorhabditis elegans | From_analysis | Panther | ||||||
| WormBase-Compara | |||||||||
| WBGene00017532 | Caenorhabditis elegans | From_analysis | Panther | ||||||
| WormBase-Compara | |||||||||
| Structured_description | Automated_description | Predicted to enable nucleoside transmembrane transporter activity. Predicted to be involved in nucleoside transmembrane transport. Located in plasma membrane. Expressed in intestine; isthmus; metacorpus; procorpus; and terminal bulb. Human ortholog(s) of this gene implicated in histiocytosis-lymphadenopathy plus syndrome. Is an ortholog of human SLC29A2 (solute carrier family 29 member 2) and SLC29A3 (solute carrier family 29 member 3). | Paper_evidence | WBPaper00065943 | |||||
| Curator_confirmed | WBPerson324 | ||||||||
| WBPerson37462 | |||||||||
| Inferred_automatically | This description was generated automatically by a script based on data from the WS291 version of WormBase | ||||||||
| Date_last_updated | 29 Nov 2023 00:00:00 | ||||||||
| Disease_info | Potential_model | DOID:0111278 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:23096) | ||||
| Molecular_info | Corresponding_CDS | K09A9.3 | |||||||
| Corresponding_transcript | K09A9.3.1 | ||||||||
| Other_sequence (19) | |||||||||
| Associated_feature (16) | |||||||||
| Experimental_info | RNAi_result | WBRNAi00034177 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00038548 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00038547 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00016865 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00050366 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Expr3056 | ||||||||
| Expr1024868 | |||||||||
| Expr1034683 | |||||||||
| Expr1154071 | |||||||||
| Expr2011324 | |||||||||
| Expr2029560 | |||||||||
| Drives_construct | WBCnstr00011105 | ||||||||
| WBCnstr00031208 | |||||||||
| Construct_product | WBCnstr00011105 | ||||||||
| WBCnstr00031208 | |||||||||
| Microarray_results (20) | |||||||||
| Expression_cluster (175) | |||||||||
| Interaction (73) | |||||||||
| Map_info | Map | X | Position | 22.9195 | Error | 0.006173 | |||
| Positive | Positive_clone | K09A9 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Mapping_data | Multi_point | 4620 | |||||||
| Pseudo_map_position | |||||||||
| Reference | WBPaper00011438 | ||||||||
| WBPaper00018608 | |||||||||
| WBPaper00024337 | |||||||||
| WBPaper00025143 | |||||||||
| WBPaper00038491 | |||||||||
| WBPaper00055090 | |||||||||
| 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 |
