WormBase Tree Display for Gene: WBGene00020422
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| WBGene00020422 | SMap | S_parent | Sequence | T10F2 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 1 | |||||||
| Name | Sequence_name | T10F2.2 | |||||||
| Molecular_name | T10F2.2 | ||||||||
| T10F2.2.1 | |||||||||
| CE02041 | |||||||||
| Other_name | CELE_T10F2.2 | Accession_evidence | NDB | BX284603 | |||||
| Public_name | T10F2.2 | ||||||||
| DB_info | Database (11) | ||||||||
| 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 (11) | |||||||||
| Strain | WBStrain00006132 | ||||||||
| WBStrain00002014 | |||||||||
| WBStrain00002140 | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation | 00056062 | ||||||||
| 00056063 | |||||||||
| 00056064 | |||||||||
| 00056065 | |||||||||
| 00056066 | |||||||||
| 00056067 | |||||||||
| Contained_in_operon | CEOP3260 | ||||||||
| Ortholog (37) | |||||||||
| Paralog (35) | |||||||||
| Structured_description | Concise_description | T10F2.2 is orthologous to the human gene SOLUTE CARRIER FAMILY 25 (MITOCHONDRIAL CARRIER; ORNITHINE TRANSPORTER) MEMBER 15 (SLC25A15; OMIM:603861), which when mutated leads to disease. | Curator_confirmed | WBPerson1823 | |||||
| WBPerson567 | |||||||||
| Date_last_updated | 06 Aug 2004 00:00:00 | ||||||||
| Automated_description | Predicted to enable L-ornithine transmembrane transporter activity. Predicted to be involved in mitochondrial L-ornithine transmembrane transport. Predicted to be located in mitochondrion. Expressed in tail. Human ortholog(s) of this gene implicated in citrullinemia and ornithine translocase deficiency. Is an ortholog of human SLC25A15 (solute carrier family 25 member 15) and SLC25A2 (solute carrier family 25 member 2). | 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:0050720 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:10985) | ||||
| DOID:9252 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:10985) | ||||||
| DOID:9273 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:10985) | ||||||
| Molecular_info | Corresponding_CDS | T10F2.2 | |||||||
| Corresponding_transcript | T10F2.2.1 | ||||||||
| Other_sequence (27) | |||||||||
| Associated_feature | WBsf226643 | ||||||||
| Experimental_info | RNAi_result | WBRNAi00018552 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00053061 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00005235 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00035448 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Chronogram848 | ||||||||
| Expr6662 | |||||||||
| Expr6663 | |||||||||
| Expr6664 | |||||||||
| Expr1023116 | |||||||||
| Expr1038906 | |||||||||
| Expr1156668 | |||||||||
| Expr2006087 | |||||||||
| Expr2024301 | |||||||||
| Drives_construct | WBCnstr00001929 | ||||||||
| WBCnstr00002797 | |||||||||
| WBCnstr00004420 | |||||||||
| WBCnstr00025153 | |||||||||
| Construct_product | WBCnstr00025153 | ||||||||
| Microarray_results (19) | |||||||||
| Expression_cluster (110) | |||||||||
| Interaction (16) | |||||||||
| Map_info | Positive | Positive_clone | T10F2 | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
| Interpolated_map_position | III | -2.04523 | |||||||
| Reference | WBPaper00038491 | ||||||||
| WBPaper00055090 | |||||||||
| Method | Gene |
