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WormBase Tree Display for Gene: WBGene00015184

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Name Class

WBGene00015184SMapS_parentSequenceB0432
IdentityVersion2
NameCGC_namedjr-1.1Person_evidenceWBPerson50
Sequence_nameB0432.2
Molecular_nameB0432.2
B0432.2.1
CE07740
Other_nameCELE_B0432.2Accession_evidenceNDBBX284602
Public_namedjr-1.1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:55WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
207 Sep 2006 09:01:01WBPerson2970Name_changeCGC_namedjr-1.1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdjr
Allele (40)
RNASeq_FPKM (74)
GO_annotation (25)
Contained_in_operonCEOP2024
Ortholog (38)
ParalogWBGene00016789Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
Structured_descriptionConcise_descriptiondjr-1.1 encodes a glyoxylase orthologous to human DJ-1 (OMIM:602533, mutated in early-onset Parkinson disease); DJR-1.1 is required for resistance to rotenone, a mitochondrial complex I inhibitor that mimics Parkinson disease (PD); djr-1.1(RNAi) animals are partly rescued from PD-like sensitivity by D-beta-hydroxybutyrate or tauroursodeoxycholic acid, and fully rescued by both; by orthology with DJ-1, DJR-1.1 may promote stability of the transcription factors SKN-1 or SKNR-1 (homologs of mammalian NFE2L2); DJR-1.1 is expressed primarily in the intestine and localizes to the nucleus and the cytoplasm.Paper_evidenceWBPaper00026906
WBPaper00028772
WBPaper00041086
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated01 May 2013 00:00:00
Automated_descriptionPredicted to enable glyoxalase III activity. Involved in several processes, including cellular aldehyde metabolic process; cellular response to aldehyde; and monocarboxylic acid biosynthetic process. Located in cytoplasm and nucleus. Expressed in intestine. Used to study Parkinson's disease. Human ortholog(s) of this gene implicated in Parkinson's disease 7; Parkinsonism; and middle cerebral artery infarction. Is an ortholog of human PARK7 (Parkinsonism associated deglycase).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_infoExperimental_modelDOID:14330Homo sapiensPaper_evidenceWBPaper00041086
Accession_evidenceOMIM606324
Curator_confirmedWBPerson324
Date_last_updated28 May 2013 00:00:00
Potential_modelDOID:0060370Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16369)
DOID:14330Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16369)
DOID:0080855Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16369)
DOID:3526Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16369)
DOID:3525Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16369)
Disease_relevanceMutations in human Park7, also known as DJ1 (orthologous to elegans djr-1.1 and djr-1.2), are associated with autosomal recessive early-onset Parkinson disease; human and worm DJ1 genes are glyoxylases, and protect neurons from reactive carbonyl species like glyoxal and methylglyoxal; studies in worms indicate that the isoforms, djr-1.1 and djr-1.2, are required for viability and protection against glyoxal-induced degeneration of dopaminergic neurons; djr-1.2 is induced under metabolic dormant states (like the dauer state in worms) induced by conditions like starvation, and is regulated by the daf-16/FoxO transcription factor, a major downstream target of the insulin-like growth factor (IGF-1) signaling pathway.Homo sapiensPaper_evidenceWBPaper00041086
Accession_evidenceOMIM602533
Curator_confirmedWBPerson324
Date_last_updated28 May 2013 00:00:00
Models_disease_in_annotationWBDOannot00000190
Molecular_infoCorresponding_CDSB0432.2
Corresponding_transcriptB0432.2.1
Other_sequence (68)
Associated_featureWBsf657259
WBsf986372
WBsf1011372
WBsf220741
WBsf220742
Experimental_infoRNAi_resultWBRNAi00098091Inferred_automaticallyRNAi_primary
WBRNAi00098087Inferred_automaticallyRNAi_primary
WBRNAi00028144Inferred_automaticallyRNAi_primary
WBRNAi00039057Inferred_automaticallyRNAi_primary
WBRNAi00098092Inferred_automaticallyRNAi_primary
WBRNAi00098089Inferred_automaticallyRNAi_primary
WBRNAi00076056Inferred_automaticallyRNAi_primary
WBRNAi00098090Inferred_automaticallyRNAi_primary
WBRNAi00009775Inferred_automaticallyRNAi_primary
Expr_patternExpr10048
Expr12289
Expr1026891
Expr1036502
Expr1143219
Expr2010935
Expr2029174
Drives_constructWBCnstr00015021
WBCnstr00017680
WBCnstr00029022
Construct_productWBCnstr00015021
WBCnstr00017680
WBCnstr00029022
Microarray_results (19)
Expression_cluster (84)
Interaction (22)
WBProcessWBbiopr:00000039
WBbiopr:00000096
Map_infoMapIIPosition-15.6463Error0.002029
PositivePositive_cloneB0432Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (19)
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