WormBase Tree Display for Gene: WBGene00020682
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| WBGene00020682 | SMap | S_parent | Sequence | T22D1 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 1 | |||||||
| Name | Sequence_name | T22D1.3 | |||||||
| Molecular_name (11) | |||||||||
| Other_name | CELE_T22D1.3 | Accession_evidence | NDB | BX284604 | |||||
| Public_name | T22D1.3 | ||||||||
| DB_info | Database (15) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 28 May 2004 13:31:03 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Allele (46) | |||||||||
| Strain | WBStrain00001687 | ||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation (19) | |||||||||
| Contained_in_operon | CEOP4204 | ||||||||
| Ortholog (45) | |||||||||
| Paralog | WBGene00017984 | Caenorhabditis elegans | From_analysis | WormBase-Compara | |||||
| Structured_description | Automated_description | Predicted to enable IMP dehydrogenase activity. Predicted to be involved in GTP biosynthetic process. Predicted to be located in cytoplasm. Expressed in head and tail. Human ortholog(s) of this gene implicated in Leber congenital amaurosis 11 and retinitis pigmentosa 10. Is an ortholog of human IMPDH1 (inosine monophosphate dehydrogenase 1). | 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:0110388 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6052) | ||||
| DOID:0110216 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6052) | ||||||
| DOID:10584 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6052) | ||||||
| Molecular_info | Corresponding_CDS | T22D1.3a | |||||||
| T22D1.3c | |||||||||
| T22D1.3e | |||||||||
| Corresponding_CDS_history | T22D1.3b:wp99 | ||||||||
| T22D1.3b:wp231 | |||||||||
| T22D1.3b:wp240 | |||||||||
| Corresponding_transcript | T22D1.3b | ||||||||
| T22D1.3d | |||||||||
| T22D1.3a.1 | |||||||||
| T22D1.3c.1 | |||||||||
| T22D1.3e.1 | |||||||||
| Other_sequence (71) | |||||||||
| Associated_feature | WBsf646051 | ||||||||
| WBsf660254 | |||||||||
| WBsf660255 | |||||||||
| WBsf228482 | |||||||||
| Experimental_info | RNAi_result | WBRNAi00069436 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00035809 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00082926 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00019022 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00053826 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Chronogram1579 | ||||||||
| Expr6744 | |||||||||
| Expr1015646 | |||||||||
| Expr1039007 | |||||||||
| Expr1157376 | |||||||||
| Expr2006365 | |||||||||
| Expr2024585 | |||||||||
| Drives_construct | WBCnstr00002511 | ||||||||
| Microarray_results (27) | |||||||||
| Expression_cluster (117) | |||||||||
| Interaction (252) | |||||||||
| Map_info | Positive | Positive_clone | T22D1 | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
| Interpolated_map_position | IV | 3.25003 | |||||||
| Reference | WBPaper00035598 | ||||||||
| WBPaper00038491 | |||||||||
| WBPaper00055090 | |||||||||
| Method | Gene |
