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WormBase Tree Display for Gene: WBGene00015297

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Name Class

WBGene00015297SMapS_parentSequenceC01F1
IdentityVersion2
NameCGC_namesco-1Person_evidenceWBPerson2601
Sequence_nameC01F1.2
Molecular_nameC01F1.2
C01F1.2.1
CE06743
Other_nameCELE_C01F1.2Accession_evidenceNDBBX284602
Public_namesco-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:55WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
218 Mar 2009 14:15:50WBPerson9133Name_changeCGC_namesco-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsco
Allele (22)
StrainWBStrain00037701
RNASeq_FPKM (74)
GO_annotation (12)
Contained_in_operonCEOP2120
Ortholog (34)
Structured_descriptionConcise_descriptionsco-1 is orthologous to the human gene SCO (CYTOCHROME OXIDASE DEFICIENT, YEAST) HOMOLOG 1 (SCO1; OMIM:603644), which when mutated leads to early-onset hepatic failure; the SCO-1 protein is predicted to be mitochondrial with 68% accuracy.Paper_evidenceWBPaper00004424
WBPaper00004637
Curator_confirmedWBPerson1843
WBPerson1823
WBPerson567
Date_last_updated18 Mar 2009 00:00:00
Automated_descriptionPredicted to enable copper chaperone activity and copper ion binding activity. Predicted to be involved in mitochondrial cytochrome c oxidase assembly. Predicted to be located in mitochondrial inner membrane. Used to study mitochondrial metabolism disease. Human ortholog(s) of this gene implicated in hypertrophic cardiomyopathy; mitochondrial complex IV deficiency nuclear type 2; and myopia. Is an ortholog of human SCO1 (synthesis of cytochrome C oxidase 1).Paper_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS291 version of WormBase
Date_last_updated29 Nov 2023 00:00:00
Disease_infoExperimental_modelDOID:700Homo sapiensPaper_evidenceWBPaper00064182
Curator_confirmedWBPerson324
Date_last_updated12 Oct 2022 00:00:00
Potential_model (5)
Models_disease_in_annotationWBDOannot00001337
Molecular_infoCorresponding_CDSC01F1.2
Corresponding_transcriptC01F1.2.1
Other_sequence (56)
Associated_featureWBsf644095
WBsf981184
WBsf221103
Experimental_infoRNAi_result (23)
Expr_patternExpr1021702
Expr1036551
Expr1143417
Expr2015645
Expr2033877
Microarray_results (20)
Expression_cluster (87)
InteractionWBInteraction000035585
WBInteraction000037559
WBInteraction000045541
WBInteraction000110277
WBInteraction000123453
WBInteraction000123454
WBInteraction000140689
WBInteraction000143729
WBInteraction000143730
WBInteraction000143731
WBInteraction000143732
WBInteraction000153210
WBInteraction000162780
WBInteraction000170247
WBInteraction000214731
WBInteraction000278428
WBInteraction000287842
WBInteraction000309320
WBInteraction000341157
WBInteraction000341158
WBInteraction000395364
WBInteraction000397987
WBInteraction000398756
WBInteraction000424519
WBInteraction000425858
WBInteraction000428703
WBInteraction000433855
WBInteraction000462219
WBInteraction000466692
WBInteraction000475396
WBInteraction000537094
WBInteraction000537188
WBInteraction000537221
WBInteraction000537254
WBInteraction000559031
WBInteraction000560087
WBInteraction000583362
WBInteraction000586757
Map_infoMapIIPosition-4.93285Error0.018941
PositivePositive_cloneC01F1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00029435
WBPaper00033751
WBPaper00038491
WBPaper00053317
WBPaper00055090
WBPaper00059862
WBPaper00061547
WBPaper00062979
WBPaper00064182
RemarkMap 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
MethodGene