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WormBase Tree Display for Gene: WBGene00020842

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Name Class

WBGene00020842SMapS_parentSequenceT27A3
IdentityVersion4
NameCGC_namenmrk-1Person_evidenceWBPerson1983
Sequence_nameT27A3.6
Molecular_nameT27A3.6
T27A3.6.1
CE14227
Other_namemoc-4Paper_evidenceWBPaper00056452
CELE_T27A3.6Accession_evidenceNDBBX284601
Public_namenmrk-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:03WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
203 Apr 2017 10:56:14WBPerson2970Name_changeCGC_namenmrk-1
312 Aug 2019 12:44:14WBPerson1983Name_changeOther_namemoc-4
411 Sep 2019 12:48:59WBPerson1983Name_changeCGC_namenmrk-1
Other_namemoc-4
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnmrk
Allele (17)
StrainWBStrain00032639
RNASeq_FPKM (74)
GO_annotation (13)
Contained_in_operonCEOP1300
Ortholog (34)
Structured_descriptionConcise_descriptionT27A3.6 is orthologous to the human gene Molybdenum cofactor synthesis gene 2 (MOCS2), which encodes molybdenum cofactor synthesis protein 2A and molybdenum cofactor synthesis protein 2B, which dimerize to form molybdopterin synthase.Paper_evidenceWBPaper00038491
Curator_confirmedWBPerson324
Date_last_updated26 Jun 2012 00:00:00
Automated_descriptionPredicted to enable molybdopterin synthase activity. Predicted to be involved in Mo-molybdopterin cofactor biosynthetic process. Predicted to be located in cytosol. Predicted to be part of molybdopterin synthase complex. Human ortholog(s) of this gene implicated in molybdenum cofactor deficiency type B. Is an ortholog of human MOCS2 (molybdenum cofactor synthesis 2).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:0111163Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7193)
Disease_relevanceMutations in the human gene Molybdenum cofactor synthesis gene 2 (MOCS2; orthologous to elegans T27A3.6), are associated with Molybdenum cofactor deficiency, type B, which is an autosomal recessive disease where there is a loss of all molybdoenzyme activities, characterized by neurological damage, seizures and early childhood death.Homo sapiensAccession_evidenceOMIM252150
603708
Curator_confirmedWBPerson324
Date_last_updated26 Jun 2012 00:00:00
Molecular_infoCorresponding_CDST27A3.6
Corresponding_transcriptT27A3.6.1
Other_sequenceCBC15288_1
CR05650
CRC00288_1
Associated_featureWBsf649219
WBsf219542
Experimental_infoRNAi_resultWBRNAi00054263Inferred_automaticallyRNAi_primary
WBRNAi00054264Inferred_automaticallyRNAi_primary
WBRNAi00036016Inferred_automaticallyRNAi_primary
WBRNAi00004319Inferred_automaticallyRNAi_primary
WBRNAi00076715Inferred_automaticallyRNAi_primary
WBRNAi00103547Inferred_automaticallyRNAi_primary
WBRNAi00116636Inferred_automaticallyRNAi_primary
Expr_patternExpr1012188
Expr1039085
Expr1157811
Expr2014334
Expr2032575
Drives_constructWBCnstr00024844
Construct_productWBCnstr00024844
Microarray_results (21)
Expression_cluster (89)
Interaction (55)
Map_infoMapIPosition0.784315
PositivePositive_cloneT27A3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00051761
WBPaper00055090
WBPaper00056452
WBPaper00064339
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