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WormBase Tree Display for Gene: WBGene00002007

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Name Class

WBGene00002007SMapS_parentSequenceC15H9
IdentityVersion1
NameCGC_namehsp-3Person_evidenceWBPerson36
Sequence_nameC15H9.6
Molecular_nameC15H9.6a
C15H9.6a.1
CE08177
C15H9.6b
CE49317
C15H9.6a.2
C15H9.6b.1
Other_namehsp70er1Paper_evidenceWBPaper00064398
CELE_C15H9.6Accession_evidenceNDBBX284606
Public_namehsp-3
DB_infoDatabaseAceViewgeneXG708
WormQTLgeneWBGene00002007
WormFluxgeneWBGene00002007
NDBlocus_tagCELE_C15H9.6
PanthergeneCAEEL|WormBase=WBGene00002007|UniProtKB=P27420
familyPTHR19375
NCBIgene180880
RefSeqproteinNM_001383595.2
NM_001307849.4
SwissProtUniProtAccP27420
TrEMBLUniProtAccV6CJ24
UniProt_GCRPUniProtAccP27420
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhsp
Allele (57)
Legacy_information[C.elegansII] NMK. Encodes protein related to mammalian grp78/BiP; not heat shock induced. [Heschl and Baillie 1990; BC]
StrainWBStrain00031808
RNASeq_FPKM (74)
GO_annotation (27)
Ortholog (53)
Paralog (11)
Structured_descriptionConcise_descriptionhsp-3 encodes one of two C. elegans heat shock response 70 (hsp70) proteins homologous to mammalian grp78/BiP (glucose regulated protein 78/immunoglobulin heavy chain-binding protein, OMIM:138120); HSP-3 likely functions as a molecular chaperone, and is expressed constitutively (expression is not heat inducible) throughout development with greatest abundance during the L1 larval stage; hsp-3 transcription is, however, upregulated in response to endoplasmic reticulum stress induced by dithiothreitol (DTT) or tunicamycin; HSP-3 contains a long hydrophobic amino terminus and a carboxyl terminal KDEL sequence suggesting that it may be retained in the endoplasmic reticulum.Paper_evidenceWBPaper00001136
WBPaper00001320
WBPaper00005044
WBPaper00031857
Curator_confirmedWBPerson1843
Date_last_updated25 Aug 2010 00:00:00
Automated_descriptionPredicted to enable ATP hydrolysis activity; heat shock protein binding activity; and protein folding chaperone. Involved in IRE1-mediated unfolded protein response. Predicted to be located in endoplasmic reticulum lumen; membrane; and nucleus. Predicted to be part of endoplasmic reticulum chaperone complex. Expressed in several structures, including germ line; hypodermis; intestinal muscle; pharyngeal-intestinal valve; and tail. Human ortholog(s) of this gene implicated in several diseases, including dopamine beta-hydroxylase deficiency; inflammatory bowel disease; and rheumatoid arthritis. Is an ortholog of human HSPA5 (heat shock protein family A (Hsp70) member 5).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:7148Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5238)
DOID:3070Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5238)
DOID:0090145Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5238)
DOID:0050589Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5238)
Molecular_infoCorresponding_CDSC15H9.6a
C15H9.6b
Corresponding_transcriptC15H9.6a.1
C15H9.6a.2
C15H9.6b.1
Other_sequence (280)
Associated_feature (25)
Experimental_infoRNAi_result (31)
Expr_pattern (11)
Drives_constructWBCnstr00002023
WBCnstr00002024
WBCnstr00009609
WBCnstr00015264
WBCnstr00019129
WBCnstr00036526
Construct_productWBCnstr00036526
Microarray_results (28)
Expression_cluster (247)
Interaction (318)
WBProcessWBbiopr:00000039
WBbiopr:00000046
WBbiopr:00000079
Map_infoMapXPosition-3.73772Error0.017656
PositivePositive_cloneBC#HS148
C15H9Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4344
4540
Pseudo_map_position
Reference (46)
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