WormBase Tree Display for Gene: WBGene00011526
expand all nodes | collapse all nodes | view schema
WBGene00011526 | SMap | S_parent | Sequence | T06D8 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||||
Name | CGC_name | cox-15 | Person_evidence | WBPerson7169 | |||||
WBPerson117 | |||||||||
Sequence_name | T06D8.5 | ||||||||
Molecular_name | T06D8.5 | ||||||||
T06D8.5.1 | |||||||||
CE02326 | |||||||||
Other_name | CELE_T06D8.5 | Accession_evidence | NDB | BX284602 | |||||
Public_name | cox-15 | ||||||||
DB_info | Database (11) | ||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 26 May 2004 16:54:52 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
2 | 22 Jan 2013 16:32:44 | WBPerson2970 | Name_change | CGC_name | cox-15 | ||||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Gene_class | cox | ||||||||
Allele (28) | |||||||||
Strain | WBStrain00051372 | ||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation | 00074672 | ||||||||
00074673 | |||||||||
00074674 | |||||||||
00074675 | |||||||||
00074676 | |||||||||
00118768 | |||||||||
00118769 | |||||||||
00118770 | |||||||||
Contained_in_operon | CEOP2524 | ||||||||
Ortholog (38) | |||||||||
Structured_description | Automated_description | Predicted to enable oxidoreductase activity, acting on NAD(P)H, heme protein as acceptor. Predicted to be involved in heme A biosynthetic process. Predicted to be located in mitochondrial inner membrane. Human ortholog(s) of this gene implicated in Leigh disease; hypertrophic cardiomyopathy; and mitochondrial complex IV deficiency nuclear type 6. Is an ortholog of human COX15 (cytochrome c oxidase assembly homolog COX15). | 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:11984 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:2263) | ||||
DOID:3652 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:2263) | ||||||
DOID:0080358 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:2263) | ||||||
Molecular_info | Corresponding_CDS | T06D8.5 | |||||||
Corresponding_transcript | T06D8.5.1 | ||||||||
Other_sequence (63) | |||||||||
Associated_feature | WBsf650552 | ||||||||
WBsf223906 | |||||||||
Experimental_info | RNAi_result | WBRNAi00000581 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00009129 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00026210 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00061564 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00052646 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00112877 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00112817 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00112937 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00033452 | Inferred_automatically | RNAi_primary | |||||||
Expr_pattern | Expr1016276 | ||||||||
Expr1035078 | |||||||||
Expr1156250 | |||||||||
Expr2010472 | |||||||||
Expr2028712 | |||||||||
Drives_construct | WBCnstr00030587 | ||||||||
Construct_product | WBCnstr00030587 | ||||||||
Microarray_results (18) | |||||||||
Expression_cluster (98) | |||||||||
Interaction (94) | |||||||||
Map_info | Map | II | Position | 3.36407 | |||||
Positive | Positive_clone | T06D8 | 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 |