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WormBase Tree Display for Gene: WBGene00013866

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Name Class

WBGene00013866SMapS_parentSequenceCHROMOSOME_X
IdentityVersion2
NameCGC_namecbs-1Paper_evidenceWBPaper00039977
Person_evidenceWBPerson537
Sequence_nameZC373.1
Molecular_nameZC373.1a
ZC373.1a.1
CE31670
ZC373.1b
CE47092
ZC373.1b.1
Other_nameCELE_ZC373.1Accession_evidenceNDBBX284606
Public_namecbs-1
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:55WBPerson1971EventImportedInitial conversion from CDS class of WS125
229 Sep 2011 10:45:56WBPerson2970Name_changeCGC_namecbs-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcbs
Allele (32)
StrainWBStrain00002826
WBStrain00052082
RNASeq_FPKM (74)
GO_annotation (16)
Ortholog (40)
Paralog (12)
Structured_descriptionConcise_descriptioncbs-1 encodes an ortholog of human CYSTATHIONINE-BETA-SYNTHASE (CBS), which when mutated leads to homocystinuria (OMIM:236200).Paper_evidenceWBPaper00004637
Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionEnables cystathionine beta-synthase activity; cysteine synthase activity; and pyridoxal phosphate binding activity. Involved in sulfur compound biosynthetic process. Located in cytoplasm. Expressed in pharyngeal muscle cell. Human ortholog(s) of this gene implicated in several diseases, including homocystinuria; hyperhomocysteinemia; and neural tube defect. Is an ortholog of human CBS (cystathionine beta-synthase).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:0080074Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1550)
DOID:12365Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1550)
DOID:9279Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1550)
DOID:9263Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1550)
DOID:3526Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1550)
DOID:3393Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1550)
Molecular_infoCorresponding_CDSZC373.1a
ZC373.1b
Corresponding_CDS_historyZC373.1:wp83
Corresponding_transcriptZC373.1a.1
ZC373.1b.1
Other_sequence (40)
Associated_featureWBsf648441
WBsf655205
WBsf1006596
WBsf236234
Experimental_infoRNAi_resultWBRNAi00058845Inferred_automaticallyRNAi_primary
WBRNAi00091457Inferred_automaticallyRNAi_primary
Expr_patternChronogram1051
Expr7160
Expr9921
Expr1018878
Expr1036202
Expr1162289
Expr2009744
Expr2027984
Drives_constructWBCnstr00003351
WBCnstr00014401
WBCnstr00029491
Construct_productWBCnstr00014401
WBCnstr00016327
WBCnstr00029491
AntibodyWBAntibody00002306
Microarray_results (22)
Expression_cluster (173)
Interaction (63)
Map_infoMapXPosition1.73547
PositivePositive_cloneZC373Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00034443
WBPaper00038491
WBPaper00040475
WBPaper00040626
WBPaper00055090
WBPaper00059856
WBPaper00059949
WBPaper00060431
WBPaper00060693
WBPaper00064989
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