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WormBase Tree Display for Gene: WBGene00008127

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Name Class

WBGene00008127SMapS_parentSequenceC47A10
IdentityVersion2
NameCGC_nameddo-1Person_evidenceWBPerson11473
Sequence_nameC47A10.5
Molecular_nameC47A10.5a
C47A10.5a.1
CE36691
C47A10.5b
CE44074
C47A10.5b.1
Other_nameCELE_C47A10.5Accession_evidenceNDBBX284605
Public_nameddo-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:48WBPerson1971EventImportedInitial conversion from CDS class of WS125
229 Apr 2010 16:43:42WBPerson2970Name_changeCGC_nameddo-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classddo
Allele (180)
RNASeq_FPKM (74)
GO_annotation (20)
Ortholog (36)
ParalogWBGene00022076Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00017648Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00017565Caenorhabditis elegansFrom_analysisInparanoid_8
Panther
WormBase-Compara
Structured_descriptionConcise_descriptionddo-1 encodes a D-aspartate oxidase (DASPO), paralogous to DDO-2 and DDO-3; recombinant DDO-1 has DASPO acvitity on acidic D-amino acid substrates (e.g., D-aspartate, D-glutamate, or N-methyl-D-aspartate/NMDA), with highest catalytic efficiency on D-glutamate; since the C-terminal residues of DDO-1 match the PTS1 consensus sequence, DDO-1 is predicted to be peroxisomal.Paper_evidenceWBPaper00028859
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated25 May 2010 00:00:00
Automated_descriptionEnables D-aspartate oxidase activity; D-glutamate oxidase activity; and FAD binding activity. Involved in obsolete oxidation-reduction process. Predicted to be located in cytoplasm. Expressed in hypodermis and intestinal cell. Human ortholog(s) of this gene implicated in schizophrenia. Is an ortholog of human DAO (D-amino acid 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:5419Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2671)
Molecular_infoCorresponding_CDSC47A10.5a
C47A10.5b
Corresponding_CDS_historyC47A10.5:wp125
Corresponding_transcriptC47A10.5a.1
C47A10.5b.1
Other_sequence (38)
Associated_featureWBsf1002742
WBsf235179
Experimental_infoRNAi_resultWBRNAi00029887Inferred_automaticallyRNAi_primary
WBRNAi00042640Inferred_automaticallyRNAi_primary
WBRNAi00012056Inferred_automaticallyRNAi_primary
Expr_patternExpr9986
Expr1021227
Expr1146627
Expr2010828
Expr2029066
Drives_constructWBCnstr00014990
WBCnstr00033218
Construct_productWBCnstr00033218
Microarray_results (18)
Expression_cluster (137)
Interaction (15)
Map_infoMapVPosition13.2002Error0.000699
PositivePositive_cloneC47A10Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00028859
WBPaper00036387
WBPaper00038491
WBPaper00040844
WBPaper00043127
WBPaper00046409
WBPaper00055090
WBPaper00059638
WBPaper00065331
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