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WormBase Tree Display for Gene: WBGene00006597

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Name Class

WBGene00006597EvidenceCGC_data_submission
SMapS_parentSequenceY37A1B
IdentityVersion1
NameCGC_nametor-1Person_evidenceWBPerson87
Sequence_nameY37A1B.12
Molecular_nameY37A1B.12
Y37A1B.12.1
CE43294
Y37A1B.12.2
Other_namedyt-2
CELE_Y37A1B.12Accession_evidenceNDBBX284604
Public_nametor-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:41WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classtor
Allele (39)
Component_of_genotypeWBGenotype00000148
RNASeq_FPKM (74)
GO_annotation (14)
Contained_in_operonCEOP4572
Ortholog (34)
ParalogWBGene00003870Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00006598Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
Structured_descriptionConcise_descriptiontor-1 encodes a AAA+ ATPase that, along with TOR-2 and OOC-5, comprise the three C. elegans orthologs of human TorsinA.Paper_evidenceWBPaper00005005
WBPaper00005722
Curator_confirmedWBPerson1843
Date_last_updated16 Jun 2008 00:00:00
Automated_descriptionPredicted to enable ATP binding activity and ATP hydrolysis activity. Predicted to be involved in cellular response to misfolded protein. Predicted to be located in endoplasmic reticulum lumen. Expressed in anal depressor muscle; head mesodermal cell; head neurons; and intestinal muscle. Human ortholog(s) of this gene implicated in arthrogryposis multiplex congenita-5 and torsion dystonia 1. Is an ortholog of human TOR1A (torsin family 1 member A) and TOR1B (torsin family 1 member B).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:0080981Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3098)
DOID:0060730Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3098)
Modifies_diseaseDOID:10652
Modifies_disease_in_annotationWBDOannot00000218
Molecular_infoCorresponding_CDSY37A1B.12
Corresponding_CDS_historyY37A1B.12:wp196
Corresponding_transcriptY37A1B.12.1
Y37A1B.12.2
Experimental_infoRNAi_resultWBRNAi00055848Inferred_automaticallyRNAi_primary
WBRNAi00076762Inferred_automaticallyRNAi_primary
Expr_patternExpr11291
Expr1020300
Expr1159379
Expr2017460
Expr2035599
Drives_constructWBCnstr00018741
WBCnstr00034281
Construct_productWBCnstr00034281
Microarray_results (15)
Expression_cluster (49)
Interaction (31)
WBProcessWBbiopr:00000078
Map_infoMapIVPosition11.0294Error0.008674
PositivePositive_cloneY37A1BInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00005005
WBPaper00005722
WBPaper00006152
WBPaper00012397
WBPaper00017955
WBPaper00017956
WBPaper00024947
WBPaper00025671
WBPaper00038491
WBPaper00055090
RemarkSequence connection from [Caldwell GA]
Map 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