Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Gene: WBGene00010397

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00010397SMapS_parentSequenceH13N06
IdentityVersion2
NameCGC_namesuox-1Person_evidenceWBPerson151
WBPerson14155
Sequence_nameH13N06.4
Molecular_nameH13N06.4a
H13N06.4a.1
CE18814
H13N06.4b
CE38383
H13N06.4c
CE54309
H13N06.4b.1
H13N06.4b.2
H13N06.4c.1
Other_nameCELE_H13N06.4Accession_evidenceNDBBX284606
Public_namesuox-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:51WBPerson1971EventImportedInitial conversion from CDS class of WS125
231 Aug 2011 09:11:34WBPerson2970Name_changeCGC_namesuox-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsuox
Allele (41)
StrainWBStrain00007976
WBStrain00051220
RNASeq_FPKM (74)
GO_annotation (14)
Contained_in_operonCEOPX136
Ortholog (38)
Structured_descriptionConcise_descriptionsuox-1 encodes a sulfite oxidase orthologous to human SUOX (SUOX; OMIM:602216), which when mutated leads to disease.Curator_confirmedWBPerson1843
WBPerson1823
WBPerson567
Date_last_updated20 Sep 2011 00:00:00
Automated_descriptionPredicted to enable heme binding activity; molybdopterin cofactor binding activity; and sulfite oxidase activity. Predicted to be involved in sulfur compound metabolic process. Predicted to be located in mitochondrion. Human ortholog(s) of this gene implicated in isolated sulfite oxidase deficiency. Is an ortholog of human SUOX (sulfite oxidase).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:0111270Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11460)
DOID:655Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11460)
Molecular_infoCorresponding_CDSH13N06.4a
H13N06.4b
H13N06.4c
Corresponding_CDS_historyH13N06.4:wp141
Corresponding_transcriptH13N06.4a.1
H13N06.4b.1
H13N06.4b.2
H13N06.4c.1
Other_sequence (49)
Associated_featureWBsf236782
Experimental_infoRNAi_resultWBRNAi00016262Inferred_automaticallyRNAi_primary
WBRNAi00027388Inferred_automaticallyRNAi_primary
WBRNAi00001187Inferred_automaticallyRNAi_primary
WBRNAi00049394Inferred_automaticallyRNAi_primary
WBRNAi00025797Inferred_automaticallyRNAi_primary
WBRNAi00033706Inferred_automaticallyRNAi_primary
WBRNAi00025798Inferred_automaticallyRNAi_primary
Expr_patternExpr1026070
Expr1034536
Expr1153127
Expr2017123
Expr2035259
Drives_constructWBCnstr00031443
Construct_productWBCnstr00031443
WBCnstr00040858
WBCnstr00040859
WBCnstr00040860
WBCnstr00040861
WBCnstr00040862
Microarray_results (28)
Expression_cluster (107)
Interaction (15)
Map_infoMapXPosition22.7267
PositivePositive_cloneH13N06Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00040475
WBPaper00055090
WBPaper00056452
WBPaper00064697
WBPaper00065026
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