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WormBase Tree Display for Gene: WBGene00011526

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Name Class

WBGene00011526SMapS_parentSequenceT06D8
IdentityVersion2
NameCGC_namecox-15Person_evidenceWBPerson7169
WBPerson117
Sequence_nameT06D8.5
Molecular_nameT06D8.5
T06D8.5.1
CE02326
Other_nameCELE_T06D8.5Accession_evidenceNDBBX284602
Public_namecox-15
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:52WBPerson1971EventImportedInitial conversion from CDS class of WS125
222 Jan 2013 16:32:44WBPerson2970Name_changeCGC_namecox-15
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcox
Allele (28)
StrainWBStrain00051372
RNASeq_FPKM (74)
GO_annotation00074672
00074673
00074674
00074675
00074676
00118768
00118769
00118770
Contained_in_operonCEOP2524
Ortholog (38)
Structured_descriptionAutomated_descriptionPredicted 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_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_infoPotential_modelDOID:11984Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2263)
DOID:3652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2263)
DOID:0080358Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2263)
Molecular_infoCorresponding_CDST06D8.5
Corresponding_transcriptT06D8.5.1
Other_sequence (63)
Associated_featureWBsf650552
WBsf223906
Experimental_infoRNAi_resultWBRNAi00000581Inferred_automaticallyRNAi_primary
WBRNAi00009129Inferred_automaticallyRNAi_primary
WBRNAi00026210Inferred_automaticallyRNAi_primary
WBRNAi00061564Inferred_automaticallyRNAi_primary
WBRNAi00052646Inferred_automaticallyRNAi_primary
WBRNAi00112877Inferred_automaticallyRNAi_primary
WBRNAi00112817Inferred_automaticallyRNAi_primary
WBRNAi00112937Inferred_automaticallyRNAi_primary
WBRNAi00033452Inferred_automaticallyRNAi_primary
Expr_patternExpr1016276
Expr1035078
Expr1156250
Expr2010472
Expr2028712
Drives_constructWBCnstr00030587
Construct_productWBCnstr00030587
Microarray_results (18)
Expression_cluster (98)
Interaction (94)
Map_infoMapIIPosition3.36407
PositivePositive_cloneT06D8Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
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