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WormBase Tree Display for Gene: WBGene00001045

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Name Class

WBGene00001045SMapS_parentSequenceY47H9C
IdentityVersion1
NameCGC_namednj-27Person_evidenceWBPerson625
Sequence_nameY47H9C.5
Molecular_nameY47H9C.5a
Y47H9C.5a.1
CE20265
Y47H9C.5b
CE40162
Y47H9C.5b.1
Other_nameCELE_Y47H9C.5Accession_evidenceNDBBX284601
Public_namednj-27
DB_infoDatabaseWormQTLgeneWBGene00001045
WormFluxgeneWBGene00001045
NDBlocus_tagCELE_Y47H9C.5
PanthergeneCAEEL|WormBase=WBGene00001045|UniProtKB=Q9XWE1
familyPTHR44340
NCBIgene173065
RefSeqproteinNM_001047239.4
NM_001047240.3
TREEFAMTREEFAM_IDTF105169
TrEMBLUniProtAccQ9XWE1
Q25AR9
UniProt_GCRPUniProtAccQ9XWE1
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:22WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdnj
Allele (171)
StrainWBStrain00001449
WBStrain00032475
RNASeq_FPKM (74)
GO_annotation (16)
Ortholog (37)
Paralog (11)
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 misfolded protein binding activity; oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor; and protein-disulfide reductase activity. Involved in IRE1-mediated unfolded protein response. Located in endoplasmic reticulum lumen. Expressed in several structures, including body wall musculature; gonadal sheath cell; intestine; rectum; and vulva. Is an ortholog of human DNAJC10 (DnaJ heat shock protein family (Hsp40) member C10).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_infoDisease_relevanceMisfolded and aggregation-prone proteins are implicated in the initiation and progression of many neurodegenerative diseases like Alzheimer''s, Parkinson''s and Huntington''s diseases; studies in transgenic elegans models of these diseases, have identified dnj-27, ortholog of mammalian ERdj5, as an endoplasmic reticulum (ER) expressed thioredoxin protein required for the degradation of misfolded proteins; RNA interference of elegans dnj-27 increases the aggregation and associated pathological phenotypes of paralysis and motility defects caused by human beta-amyloid peptide, human alpha-synuclein and polyglutamine (polyQ) proteins, while overexpression of elegans dnj-27 ameliorates the phenotypes; further dnj-27 down-regulation alters cytoplasmic protein homeostasis and causes mitochondrial fragmentation.Homo sapiensPaper_evidenceWBPaper00042360
Curator_confirmedWBPerson324
Date_last_updated23 Jan 2015 00:00:00
Molecular_infoCorresponding_CDSY47H9C.5a
Y47H9C.5b
Corresponding_transcriptY47H9C.5a.1
Y47H9C.5b.1
Other_sequence (21)
Associated_featureWBsf654829
WBsf985404
WBsf985405
WBsf985406
WBsf1010799
WBsf1010800
WBsf1010801
WBsf1010802
WBsf218564
Experimental_infoRNAi_resultWBRNAi00037210Inferred_automaticallyRNAi_primary
WBRNAi00108398Inferred_automaticallyRNAi_primary
WBRNAi00056850Inferred_automaticallyRNAi_primary
WBRNAi00108375Inferred_automaticallyRNAi_primary
WBRNAi00108379Inferred_automaticallyRNAi_primary
WBRNAi00106342Inferred_automaticallyRNAi_primary
WBRNAi00108378Inferred_automaticallyRNAi_primary
WBRNAi00058311Inferred_automaticallyRNAi_primary
Expr_patternExpr6995
Expr11009
Expr1027217
Expr1030657
Expr1160301
Expr2011002
Expr2029240
Drives_constructWBCnstr00002331
WBCnstr00017696
WBCnstr00017697
WBCnstr00017698
WBCnstr00017980
WBCnstr00017981
Construct_productWBCnstr00017980
WBCnstr00017981
WBCnstr00038139
AntibodyWBAntibody00002463
Microarray_results (26)
Expression_cluster (168)
Interaction (30)
WBProcessWBbiopr:00000076
Map_infoMapIPosition12.892Error0.004864
PositivePositive_cloneY47H9CInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00036931
WBPaper00038491
WBPaper00039115
WBPaper00042360
WBPaper00055090
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