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WormBase Tree Display for Gene: WBGene00001042

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Name Class

WBGene00001042SMapS_parentSequenceW03A5
IdentityVersion1
NameCGC_namednj-24Person_evidenceWBPerson625
Sequence_nameW03A5.7
Molecular_nameW03A5.7
W03A5.7.1
CE38983
W03A5.7.2
Other_nameCELE_W03A5.7Accession_evidenceNDBBX284603
Public_namednj-24
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:22WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdnj
Allele (104)
RNASeq_FPKM (74)
GO_annotation00097392
00097393
00097394
00097395
00097396
00097397
00097398
00108149
00108150
00108151
Ortholog (53)
ParalogWBGene00001036
WBGene00001019Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001022Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001031Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001034Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001038Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001040Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001044Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionThis gene encodes a protein containing a DnaJ ('J') domain.Paper_evidenceWBPaper00012768
WBPaper00012859
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable protein folding chaperone; protein-folding chaperone binding activity; and unfolded protein binding activity. Predicted to be involved in chaperone-mediated protein folding. Located in nucleus. Human ortholog(s) of this gene implicated in autosomal dominant limb-girdle muscular dystrophy type 1 and distal spinal muscular atrophy type 5. Is an ortholog of human DNAJB8 (DnaJ heat shock protein family (Hsp40) member B8).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:0111214Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5228)
DOID:0110305Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14888)
Molecular_infoCorresponding_CDSW03A5.7
Corresponding_CDS_historyW03A5.7:wp146
Corresponding_transcriptW03A5.7.1
W03A5.7.2
Other_sequence (26)
Associated_feature (15)
Experimental_infoRNAi_resultWBRNAi00019536Inferred_automaticallyRNAi_primary
WBRNAi00106339Inferred_automaticallyRNAi_primary
WBRNAi00006686Inferred_automaticallyRNAi_primary
WBRNAi00054651Inferred_automaticallyRNAi_primary
WBRNAi00112268Inferred_automaticallyRNAi_primary
WBRNAi00076733Inferred_automaticallyRNAi_primary
Expr_patternExpr9507
Expr1016901
Expr1030654
Expr1158194
Expr2010999
Expr2029237
Drives_constructWBCnstr00037122
Construct_productWBCnstr00014072
WBCnstr00037122
Microarray_results (22)
Expression_cluster (114)
Interaction (19)
Map_infoMapIIIPosition-1.71976Error0.011053
PositivePositive_cloneW03A5Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038444
WBPaper00038491
WBPaper00050564
WBPaper00055090
WBPaper00061766
WBPaper00064214
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