WormBase Tree Display for Gene: WBGene00002071
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| WBGene00002071 | Evidence | Person_evidence | WBPerson842 | ||||||
|---|---|---|---|---|---|---|---|---|---|
| SMap | S_parent | Sequence | T04G9 | ||||||
| Identity | Version | 1 | |||||||
| Name | CGC_name | ile-2 | Person_evidence | WBPerson842 | |||||
| Sequence_name | T04G9.3 | ||||||||
| Molecular_name | T04G9.3 | ||||||||
| T04G9.3.1 | |||||||||
| CE23946 | |||||||||
| Other_name | CELE_T04G9.3 | Accession_evidence | NDB | BX284606 | |||||
| Public_name | ile-2 | ||||||||
| DB_info | Database (11) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 07 Apr 2004 11:29:26 | WBPerson1971 | Event | Imported | Initial conversion from geneace | ||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | ile | ||||||||
| Allele (28) | |||||||||
| Strain | WBStrain00051369 | ||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation | 00074411 | ||||||||
| 00074412 | |||||||||
| 00074413 | |||||||||
| 00074414 | |||||||||
| 00074415 | |||||||||
| 00074416 | |||||||||
| 00074417 | |||||||||
| 00109968 | |||||||||
| Ortholog (42) | |||||||||
| Paralog | WBGene00002070 | Caenorhabditis elegans | From_analysis | Panther | |||||
| WormBase-Compara | |||||||||
| Structured_description | Automated_description | Predicted to enable mannose binding activity. Predicted to be involved in endoplasmic reticulum to Golgi vesicle-mediated transport. Predicted to be located in intracellular membrane-bounded organelle. Human ortholog(s) of this gene implicated in autosomal dominant intellectual developmental disorder and autosomal recessive intellectual developmental disorder 52. Is an ortholog of human LMAN2 (lectin, mannose binding 2) and LMAN2L (lectin, mannose binding 2 like). | 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:0060307 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:19263) | ||||
| DOID:0081215 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:19263) | ||||||
| Molecular_info | Corresponding_CDS | T04G9.3 | |||||||
| Corresponding_transcript | T04G9.3.1 | ||||||||
| Other_sequence (31) | |||||||||
| Associated_feature | WBsf655145 | ||||||||
| WBsf662435 | |||||||||
| WBsf235279 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00092916 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00018152 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00076644 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00035148 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00052409 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Expr1027190 | ||||||||
| Expr1031224 | |||||||||
| Expr1156034 | |||||||||
| Expr2012719 | |||||||||
| Expr2030955 | |||||||||
| Drives_construct | WBCnstr00036476 | ||||||||
| Construct_product | WBCnstr00036476 | ||||||||
| Microarray_results (19) | |||||||||
| Expression_cluster (124) | |||||||||
| Interaction (28) | |||||||||
| Map_info | Map | X | Position | -19.5012 | |||||
| Positive | Positive_clone | T04G9 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Pseudo_map_position | |||||||||
| Reference | 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 |
